A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570947



Internal ID16011670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:272935..297326hg38UCSC Ensembl
Innerchr16:322934..347326hg19UCSC Ensembl
Innerchr16:262935..287327hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3824392
hg1924393
hg1824393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851300
Samples
Known GenesARHGDIG, AXIN1, PDIA2, RGS11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570947
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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