A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522572



Internal ID15449865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49865615..49881644hg38UCSC Ensembl
Innerchr2:50092753..50108782hg19UCSC Ensembl
Innerchr2:49946257..49962286hg18UCSC Ensembl
Innerchr2:50004404..50020433hg17UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3816030
hg1916030
hg1816030
hg1716030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705956
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522572
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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