A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525598



Internal ID15452891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49928495..49936052hg38UCSC Ensembl
Innerchr16:49962406..49969963hg19UCSC Ensembl
Innerchr16:48519907..48527464hg18UCSC Ensembl
Innerchr16:48519907..48527464hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg387558
hg197558
hg187558
hg177558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701741
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525598
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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