A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572509



Internal ID16359918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46418653..46465264hg38UCSC Ensembl
Innerchr16:46452565..46499176hg19UCSC Ensembl
Innerchr16:45010066..45056677hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3846612
hg1946612
hg1846612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5105n54
Supporting Variantsnssv856609, nssv856610
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572509
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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