A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632565



Internal ID7019375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67746807..67755711hg38UCSC Ensembl
chr13:68320939..68329843hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg388905
hg198905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14782209, essv14782215, essv14782223, essv14782212, essv14782207, essv14782210, essv14782221, essv14782219, essv14782214, essv14782222, essv14782225, essv14782217, essv14782211, essv14782218, essv14782216, essv14782226, essv14782213, essv14782220, essv14782224, essv14782208
SamplesHG03514, NA19703, HG02419, HG03193, HG02952, NA19038, NA18871, HG02508, HG03294, HG03064, NA18909, NA18517, HG02501, NA19037, HG03469, NA19438, NA19474, HG03351, HG03445, HG02763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632565
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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