A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573409



Internal ID16014132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83940461..83975847hg38UCSC Ensembl
Innerchr16:83974066..84009452hg19UCSC Ensembl
Innerchr16:82531567..82566953hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3835387
hg1935387
hg1835387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv861994
Samples
Known GenesNECAB2, OSGIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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