A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636797



Internal ID7023591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67918626..67919334hg38UCSC Ensembl
Innerchr15:67918636..67919324hg38UCSC Ensembl
Outerchr15:67918616..67919344hg38UCSC Ensembl
chr15:68210964..68211672hg19UCSC Ensembl
Innerchr15:68210974..68211662hg19UCSC Ensembl
Outerchr15:68210954..68211682hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15279292, essv15279290, essv15279291, essv15279289, essv15279288, essv15279295, essv15279294, essv15279297, essv15279293, essv15279296
SamplesHG01986, HG02628, HG02702, HG03572, HG02840, HG02143, HG03380, NA18908, HG02947, HG02851
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636797
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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