A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516425



Internal ID15443718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2690980..2790307hg38UCSC Ensembl
Innerchr9:2690980..2790307hg19UCSC Ensembl
Innerchr9:2680980..2780307hg18UCSC Ensembl
Innerchr9:2680980..2780307hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3899328
hg1999328
hg1899328
hg1799328
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657571, nssv700988, nssv668287, nssv694552, nssv699054, nssv668433, nssv694398, nssv662583, nssv674844
Samples
Known GenesKCNV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516425
Frequency
Sample Size2026
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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