A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573467



Internal ID16014190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84809371..84874236hg38UCSC Ensembl
Innerchr16:84842977..84907842hg19UCSC Ensembl
Innerchr16:83400478..83465343hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3864866
hg1964866
hg1864866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5269n54
Supporting Variantsnssv862183, nssv862182
Samples
Known GenesCRISPLD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573467
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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