A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527537



Internal ID15108144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24056887..24056993hg38UCSC Ensembl
Innerchr16:24068208..24068314hg19UCSC Ensembl
Innerchr16:23975709..23975815hg18UCSC Ensembl
Innerchr16:23975709..23975815hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38107
hg19107
hg18107
hg17107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703998
Samples
Known GenesPRKCB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527537
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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