A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524914



Internal ID15452207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86057292..86058024hg38UCSC Ensembl
Innerchr16:86090898..86091630hg19UCSC Ensembl
Innerchr16:84648399..84649131hg18UCSC Ensembl
Innerchr16:84648399..84649131hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38733
hg19733
hg18733
hg17733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700926
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524914
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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