A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594646



Internal ID16035369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70240300..70271806hg38UCSC Ensembl
Innerchr4:71106017..71137523hg19UCSC Ensembl
Innerchr4:71140606..71172112hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3831507
hg1931507
hg1831507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1002279
Samples
Known GenesCSN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594646
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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