A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525656



Internal ID15452949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63747727..63749652hg38UCSC Ensembl
Innerchr16:63781631..63783556hg19UCSC Ensembl
Innerchr16:62339132..62341057hg18UCSC Ensembl
Innerchr16:62339132..62341057hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381926
hg191926
hg181926
hg171926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701811
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525656
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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