A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517380



Internal ID15444673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17564269..17633234hg38UCSC Ensembl
Innerchr9:17564267..17633232hg19UCSC Ensembl
Innerchr9:17554267..17623232hg18UCSC Ensembl
Innerchr9:17554267..17623232hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3868966
hg1968966
hg1868966
hg1768966
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701429, nssv666605, nssv675357, nssv651859, nssv672798, nssv656453, nssv692769, nssv692590
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517380
Frequency
Sample Size2026
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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