A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861695



Internal ID16155651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79574511..79612092hg38UCSC Ensembl
Innerchr16:79608408..79645989hg19UCSC Ensembl
Innerchr16:78165909..78203490hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3837582
hg1937582
hg1837582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573289
Supporting Variants
Samples
Known GenesMAF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer