A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571034



Internal ID16358443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:767339..774098hg38UCSC Ensembl
Innerchr16:817339..824098hg19UCSC Ensembl
Innerchr16:757340..764099hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386760
hg196760
hg186760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851820, nssv851819, nssv851818, nssv851821
Samples
Known GenesMIR662, MSLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571034
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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