A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852794



Internal ID16146750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954988..14990418hg38UCSC Ensembl
Innerchr16:15048845..15084275hg19UCSC Ensembl
Innerchr16:14956346..14991776hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3835431
hg1935431
hg1835431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571521
Supporting Variants
Samples
Known GenesPDXDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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