A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573472



Internal ID16014195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84891388..84909613hg38UCSC Ensembl
Innerchr16:84924994..84943219hg19UCSC Ensembl
Innerchr16:83482495..83500720hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3818226
hg1918226
hg1818226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149342
SamplesHGDP01217
Known GenesCRISPLD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573472
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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