A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593904



Internal ID16381313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32526374..32576107hg38UCSC Ensembl
Innerchr4:32527996..32577729hg19UCSC Ensembl
Innerchr4:32171894..32221627hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3849734
hg1949734
hg1849734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995200
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593904
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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