A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702961



Internal ID15439613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18698911..19116208hg38UCSC Ensembl
Innerchr6:18699142..19116439hg19UCSC Ensembl
Innerchr6:18807121..19224418hg18UCSC Ensembl
Innerchr6:18807121..19224418hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38417298
hg19417298
hg18417298
hg17417298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526639
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702961
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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