A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571699



Internal ID16012422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23923570..23929919hg38UCSC Ensembl
Innerchr16:23934891..23941240hg19UCSC Ensembl
Innerchr16:23842392..23848741hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386350
hg196350
hg186350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4959n54
Supporting Variantsnssv854189, nssv854190, nssv854188
Samples
Known GenesPRKCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571699
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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