A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657167



Internal ID9576586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86385842..86385998hg38UCSC Ensembl
chr1:86851525..86851681hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5912079, essv5944962, essv6029897, essv5679548, essv6141134, essv5669557, essv5918673, essv5483860, essv5771695, essv5941848, essv6058453, essv5927908, essv5937689, essv5755320, essv5717916, essv5997429, essv5904158, essv5423180, essv5812776, essv6369036, essv6449223, essv5535295, essv5434742, essv5521779, essv5525644, essv6261292, essv5883364, essv5831353, essv6486775, essv5814412, essv6347556, essv6030565, essv5510722, essv6004440
SamplesHG00613, HG00596, HG00310, NA18948, HG00614, NA18947, NA19210, NA11994, NA18623, NA18617, HG00689, HG00330, NA19066, HG00584, NA18537, NA18620, HG01191, NA18486, NA18977, HG00478, HG00513, HG00524, HG00512, NA18940, HG00608, NA18944, NA18571, HG00324, NA18549, NA18574, HG00684, HG00704, NA18555, NA18553
Known GenesODF2L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657167
Frequency
Sample Size1151
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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