A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519267



Internal ID15446560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38710617..38711071hg38UCSC Ensembl
Innerchr9:38710614..38711068hg19UCSC Ensembl
Innerchr9:38700614..38701068hg18UCSC Ensembl
Innerchr9:38700614..38701068hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38455
hg19455
hg18455
hg17455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691638, nssv655138, nssv684962
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519267
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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