A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517269



Internal ID15097876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26945978..27137244hg38UCSC Ensembl
Innerchr9:26945976..27137242hg19UCSC Ensembl
Innerchr9:26935976..27127242hg18UCSC Ensembl
Innerchr9:26935976..27127242hg17UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38191267
hg19191267
hg18191267
hg17191267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682582, nssv681883, nssv670112, nssv654170
Samples
Known GenesIFT74, LRRC19, PLAA, TEK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517269
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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