A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571582



Internal ID16012305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19038056..19790801hg38UCSC Ensembl
Innerchr16:19049378..19802123hg19UCSC Ensembl
Innerchr16:18956879..19709624hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38752746
hg19752746
hg18752746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852872
Samples
Known GenesC16orf62, CCP110, CLEC19A, COQ7, GDE1, IQCK, ITPRIPL2, KNOP1, SYT17, TMC5, TMC7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571582
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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