A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861699



Internal ID16155655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80217368..80307218hg38UCSC Ensembl
Innerchr16:80251265..80341115hg19UCSC Ensembl
Innerchr16:78808766..78898616hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3889851
hg1989851
hg1889851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573295
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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