A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522918



Internal ID15103525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:160153991..160180340hg38UCSC Ensembl
Innerchr1:160123781..160150130hg19UCSC Ensembl
Innerchr1:158390405..158416754hg18UCSC Ensembl
Innerchr1:156936854..156963203hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3826350
hg1926350
hg1826350
hg1726350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698579
Samples
Known GenesATP1A4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522918
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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