A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv858913



Internal ID16152869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:61474682..61561412hg38UCSC Ensembl
Innerchr16:61508586..61595316hg19UCSC Ensembl
Innerchr16:60066087..60152817hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3886731
hg1986731
hg1886731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572843
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)nssv858913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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