A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572915



Internal ID16360324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70123665..70157430hg38UCSC Ensembl
Innerchr16:70157568..70191333hg19UCSC Ensembl
Innerchr16:68715069..68748834hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3833766
hg1933766
hg1833766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5178n54
Supporting Variantsnssv859081
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572915
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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