A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856607



Internal ID16150563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46418653..46465100hg38UCSC Ensembl
Innerchr16:46452565..46499012hg19UCSC Ensembl
Innerchr16:45010066..45056513hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3846448
hg1946448
hg1846448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572508
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)nssv856607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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