A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516266



Internal ID15443559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91696387..91714136hg38UCSC Ensembl
Innerchr9:94458669..94476418hg19UCSC Ensembl
Innerchr9:93498490..93516239hg18UCSC Ensembl
Innerchr9:91538224..91555973hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3817750
hg1917750
hg1817750
hg1717750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv490n21
Supporting Variantsnssv667191, nssv678209, nssv659910, nssv690859
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516266
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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