A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017968



Internal ID16311924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184825633..184826321hg38UCSC Ensembl
Innerchr4:185746787..185747475hg19UCSC Ensembl
Innerchr4:185983781..185984469hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38689
hg19689
hg18689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596360
Supporting Variants
Samples
Known GenesACSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017968
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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