A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572948



Internal ID16013671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70690529..70697967hg38UCSC Ensembl
Innerchr16:70724432..70731870hg19UCSC Ensembl
Innerchr16:69281933..69289371hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg387439
hg197439
hg187439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859121
Samples
Known GenesVAC14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572948
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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