A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677786



Internal ID9943891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:80228726..80234401hg38UCSC Ensembl
Outerchr15:80228539..80234581hg38UCSC Ensembl
Innerchr15:80521068..80526743hg19UCSC Ensembl
Outerchr15:80520881..80526923hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg386043
hg196043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5966671, essv6443790, essv5417059, essv6531455, essv5855768, essv6523193, essv5556605, essv5527447, essv5733553, essv5611481
SamplesNA18616, HG00501, HG00534, NA18557, HG00530, HG00419, HG00556, NA18579, NA18632, NA18549
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677786
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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