A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572969



Internal ID16360378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:73630849..74007822hg38UCSC Ensembl
Innerchr16:73664748..74041721hg19UCSC Ensembl
Innerchr16:72222249..72599222hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38376974
hg19376974
hg18376974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149714
SamplesHGDP00552
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572969
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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