A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522243



Internal ID15449536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87246209..87255170hg38UCSC Ensembl
Innerchr1:87711892..87720853hg19UCSC Ensembl
Innerchr1:87484480..87493441hg18UCSC Ensembl
Innerchr1:87423913..87432874hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg388962
hg198962
hg188962
hg178962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695023
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522243
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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