A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1178e199



Internal ID22758951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1664109..1668456hg38UCSC Ensembl
chr7:1703745..1708092hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg384348
hg194348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672578, esv2660161
SamplesNA19394, NA18502, NA19397, NA19466, NA19204, NA18861, NA18508, NA19399, NA19332, NA18507, NA18917, NA19350, NA19359, NA18486, NA19355, NA19393, NA18504, NA19377, NA19443, NA19190, NA19098, NA18870, NA18510, NA19107, NA19446, NA19374, NA19396, NA19381, NA19373, NA19171, NA18519, NA19382, NA19315, NA18489, NA19448, NA19119, NA18923, NA19198, NA19131, NA18916, NA19457, NA19313, NA19138, NA18498, NA19384, NA19130, NA19383, NA18874, NA18868, NA19137, NA19372, NA19371, NA19235, NA19207, NA19172, NA19471, NA19317, NA19159, NA19189, NA18520, NA19209, NA19445, NA18908, NA18867, NA19451, NA19200, NA19247, NA18934, NA19462, NA19347, NA19152, NA19391, NA19455, NA19236, NA18516, NA18910, NA18871, NA18907, NA19461, NA19114, NA19449, NA18499, NA18856, NA19453, NA18912, NA18853, NA19099, NA19338, NA19257, NA19452, NA18523, NA19469, NA19160, NA18858, NA19436, NA19401, NA19375, NA19440, NA18909, NA19108, NA19256, NA19434, NA19473, NA19435, NA19444, NA19334, NA19439, NA19470, NA19311, NA19467, NA19360, NA19398, NA18501, NA19248, NA19438, NA19472, NA19468, NA19474, NA19093, NA19102, NA18873, NA19116, NA19213, NA19430, NA19129, NA19316, NA19312, NA19463, NA18511, NA18522, NA19429, NA19346, NA18487, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1178e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss134
Observed Complex0
Frequencyn/a


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