A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv858906



Internal ID16152862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59544657..59722663hg38UCSC Ensembl
Innerchr16:59578561..59756567hg19UCSC Ensembl
Innerchr16:58136062..58314068hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38178007
hg19178007
hg18178007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572832
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)nssv858906
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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