A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656756



Internal ID9922861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175844747..175845002hg38UCSC Ensembl
chr2:176709475..176709730hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5405395, essv6072429, essv6342146, essv5432505, essv6238409, essv6057036, essv5814355, essv5564366, essv5683266, essv5699899, essv5926228, essv6376309, essv5402371, essv6298639, essv5627136, essv6303636, essv5682522, essv5869066, essv6450422, essv6585707, essv6014785, essv5912862, essv6083953, essv6557422, essv6595126, essv5844126, essv6142746, essv5401098, essv5481230, essv5404814, essv5468014, essv6126923, essv5463259, essv6556152, essv5615576, essv5720969, essv5591084, essv5822437, essv6579044, essv5657011, essv5886802, essv5946094, essv6417001, essv6221936, essv6523286, essv5886063, essv5436038, essv5702776, essv5991702, essv5813742, essv5979818, essv5412687, essv6388205, essv5552259, essv6472080, essv5502676, essv5838760, essv5787045, essv6591733, essv6320681, essv6249102, essv5720503, essv6372508, essv5630925, essv6018245, essv5725307, essv5690076, essv5660408, essv6496559, essv6009908, essv6467351, essv6521915, essv6131623, essv5864210, essv6425553, essv5400976, essv5800663, essv6188549, essv6190418, essv5554669, essv6430711, essv6037617, essv5458731, essv5675135, essv5428920, essv5549337, essv5923761, essv5790549, essv6107096, essv5933423, essv6500332, essv6080281, essv5539079, essv6543415
SamplesNA18502, HG00442, NA18924, HG01359, NA19332, NA19359, NA18486, NA19355, NA19057, NA18596, HG00663, NA19396, HG00127, NA19373, NA19005, NA18550, NA19448, NA18942, NA07048, NA19197, NA19457, NA18571, HG00270, HG01365, HG00185, HG00281, NA19372, NA12044, HG00534, NA19385, NA19239, HG01133, NA12828, NA19445, NA20757, NA19921, NA19451, HG00464, NA18605, NA19210, NA19657, HG00428, NA20809, NA19717, HG00263, NA18579, NA19658, HG00708, NA19461, NA19114, NA19449, HG00690, HG00331, NA11894, HG01101, NA18555, HG00146, HG01107, NA19675, NA18632, NA19390, NA18909, NA19321, NA18543, NA19434, NA12775, NA19747, HG00366, NA19240, NA19380, HG00607, NA19679, NA19439, NA19311, NA18615, HG00620, HG00339, NA19398, HG00672, NA19438, HG00656, NA19093, NA20786, NA19116, HG00343, NA20528, HG00372, HG00274, HG00595, HG01082, NA19312, HG00345, NA07000, HG01112
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656756
Frequency
Sample Size1151
Observed Gain0
Observed Loss94
Observed Complex0
Frequencyn/a


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