A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571310



Internal ID16358719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5654840..5951021hg38UCSC Ensembl
Innerchr16:5704841..6001022hg19UCSC Ensembl
Innerchr16:5644842..5941023hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38296182
hg19296182
hg18296182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852349, nssv852348, nssv852350
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571310
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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