A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861939



Internal ID16155895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81559329..81575693hg38UCSC Ensembl
Innerchr16:81592934..81609298hg19UCSC Ensembl
Innerchr16:80150435..80166799hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3816365
hg1916365
hg1816365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573362
Supporting Variants
Samples
Known GenesCMIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861939
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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