A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859066



Internal ID16153022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64151126..64187114hg38UCSC Ensembl
Innerchr16:64185030..64221018hg19UCSC Ensembl
Innerchr16:62742531..62778519hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3835989
hg1935989
hg1835989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572897
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)nssv859066
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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