A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598192



Internal ID16038915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:56815165..56816270hg38UCSC Ensembl
Innerchr5:56110992..56112097hg19UCSC Ensembl
Innerchr5:56146749..56147854hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381106
hg191106
hg181106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9790n54
Supporting Variantsnssv1030744
Samples
Known GenesMAP3K1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598192
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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