A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570949



Internal ID16358358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:279671..284580hg38UCSC Ensembl
Innerchr16:329671..334580hg19UCSC Ensembl
Innerchr16:269672..274581hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384910
hg194910
hg184910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851302
Samples
Known GenesARHGDIG, PDIA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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