A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv858912



Internal ID16152868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:61265257..61418650hg38UCSC Ensembl
Innerchr16:61299161..61452554hg19UCSC Ensembl
Innerchr16:59856662..60010055hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38153394
hg19153394
hg18153394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572842
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)nssv858912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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