A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525510



Internal ID15106117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21481557..21484696hg38UCSC Ensembl
Innerchr9:21481556..21484695hg19UCSC Ensembl
Innerchr9:21471556..21474695hg18UCSC Ensembl
Innerchr9:21471556..21474695hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg383140
hg193140
hg183140
hg173140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701643
Samples
Known GenesIFNE, MIR31HG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525510
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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