A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852777



Internal ID16146733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13547001..13604118hg38UCSC Ensembl
Innerchr16:13640858..13697975hg19UCSC Ensembl
Innerchr16:13548359..13605476hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3857118
hg1957118
hg1857118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571506
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)nssv852777
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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