A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610567



Internal ID6997484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120660674..120688773hg38UCSC Ensembl
Innerchr6:120660674..120688773hg38UCSC Ensembl
Outerchr6:120660174..120689273hg38UCSC Ensembl
chr6:120981820..121009919hg19UCSC Ensembl
Innerchr6:120981820..121009919hg19UCSC Ensembl
Outerchr6:120981320..121010419hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3828100
hg1928100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1214e214
Supporting Variantsessv12524387, essv12524386, essv12524385
SamplesNA18605, HG00623, NA18957
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610567
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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