A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859051



Internal ID16153007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62861861..62989277hg38UCSC Ensembl
Innerchr16:62895765..63023181hg19UCSC Ensembl
Innerchr16:61453266..61580682hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38127417
hg19127417
hg18127417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572877
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)nssv859051
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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