A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572935



Internal ID16013658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70158702..70162064hg38UCSC Ensembl
Innerchr16:70192605..70195967hg19UCSC Ensembl
Innerchr16:68750106..68753468hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383363
hg193363
hg183363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859105
Samples
Known GenesPDPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572935
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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