A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525220



Internal ID15105827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2868291..2869928hg38UCSC Ensembl
Innerchr16:2918292..2919929hg19UCSC Ensembl
Innerchr16:2858293..2859930hg18UCSC Ensembl
Innerchr16:2858293..2859930hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381638
hg191638
hg181638
hg171638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701306
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525220
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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