A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571520



Internal ID16358929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954988..14986485hg38UCSC Ensembl
Innerchr16:15048845..15080342hg19UCSC Ensembl
Innerchr16:14956346..14987843hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3831498
hg1931498
hg1831498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4921n54
Supporting Variantsnssv852791
Samples
Known GenesPDXDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571520
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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