A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573466



Internal ID16014189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84792330..84895125hg38UCSC Ensembl
Innerchr16:84825936..84928731hg19UCSC Ensembl
Innerchr16:83383437..83486232hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38102796
hg19102796
hg18102796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149340
SamplesHGDP00766
Known GenesCRISPLD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573466
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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