A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667820



Internal ID15057786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69808822..69820364hg38UCSC Ensembl
Innerchr10:71568578..71580120hg19UCSC Ensembl
Innerchr10:71238584..71250126hg18UCSC Ensembl
Innerchr10:71238584..71250126hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3811543
hg1911543
hg1811543
hg1711543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516370
Supporting Variants
Samples
Known GenesCOL13A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667820
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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