A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521116



Internal ID15448409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101880684..102142172hg38UCSC Ensembl
Innerchr9:104642966..104904454hg19UCSC Ensembl
Innerchr9:103682787..103944275hg18UCSC Ensembl
Innerchr9:101722521..101984009hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38261489
hg19261489
hg18261489
hg17261489
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682410, nssv699204, nssv700677, nssv688920
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521116
Frequency
Sample Size2026
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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