A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516680



Internal ID15443973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90354662..90376318hg38UCSC Ensembl
Innerchr9:93116944..93138600hg19UCSC Ensembl
Innerchr9:92156764..92178420hg18UCSC Ensembl
Innerchr9:90196498..90218154hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3821657
hg1921657
hg1821657
hg1721657
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659095, nssv670114, nssv678979, nssv703021
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516680
Frequency
Sample Size2026
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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