A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526225



Internal ID8420500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72987987..73372263hg38UCSC Ensembl
Innerchr9:75602903..75987179hg19UCSC Ensembl
Innerchr9:74792723..75176999hg18UCSC Ensembl
Innerchr9:72832457..73216733hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38384277
hg19384277
hg18384277
hg17384277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702491
Samples
Known GenesANXA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526225
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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