A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526432



Internal ID15453725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101407309..101417319hg38UCSC Ensembl
Innerchr1:101872865..101882875hg19UCSC Ensembl
Innerchr1:101645453..101655463hg18UCSC Ensembl
Innerchr1:101584886..101594896hg17UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3810011
hg1910011
hg1810011
hg1710011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702735
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526432
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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