A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573304



Internal ID16360713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80921496..80955962hg38UCSC Ensembl
Innerchr16:80955393..80989859hg19UCSC Ensembl
Innerchr16:79512894..79547360hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3834467
hg1934467
hg1834467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5239n54
Supporting Variantsnssv1149309, nssv1149308
SamplesHGDP00994, HGDP01408
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573304
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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