A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527768



Internal ID15455061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:26645632..26649109hg38UCSC Ensembl
Innerchr16:26656953..26660430hg19UCSC Ensembl
Innerchr16:26564454..26567931hg18UCSC Ensembl
Innerchr16:26564454..26567931hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383478
hg193478
hg183478
hg173478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704257
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527768
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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