A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521535



Internal ID15102142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4687677..4712657hg38UCSC Ensembl
Innerchr1:4747737..4772717hg19UCSC Ensembl
Innerchr1:4647597..4672577hg18UCSC Ensembl
Innerchr1:4658110..4683090hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3824981
hg1924981
hg1824981
hg1724981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694458
Samples
Known GenesAJAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521535
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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