A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572535



Internal ID16013258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46465368..46471927hg38UCSC Ensembl
Innerchr16:46499280..46505839hg19UCSC Ensembl
Innerchr16:45056781..45063340hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg386560
hg196560
hg186560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv856647
Samples
Known GenesANKRD26P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572535
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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