A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656557



Internal ID9575976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159665384..159668790hg38UCSC Ensembl
Outerchr6:159665013..159669160hg38UCSC Ensembl
Innerchr6:160086416..160089822hg19UCSC Ensembl
Outerchr6:160086045..160090192hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384148
hg194148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6177199, essv5953627, essv6269002, essv5454713, essv5780413, essv5471204, essv5798857, essv5438877, essv5666434, essv5711714, essv6146358, essv6561896, essv6421218, essv5646772, essv5404632, essv5804806, essv5704050, essv6305520, essv5638660, essv6226372, essv6116865, essv6331058, essv5445921, essv6548366, essv6467794, essv6547057, essv5542220, essv6197993
SamplesHG00361, HG00318, HG00327, HG00270, HG00334, HG00277, HG00309, HG00338, HG00178, HG00323, HG00188, HG00266, HG00183, HG00176, HG00282, HG00328, HG00320, HG00275, HG00324, HG00373, HG00276, HG00353, HG00267, HG00310, HG00186, HG00377, HG00372, HG00180
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656557
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer