A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017028



Internal ID15964298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176110774..176225476hg38UCSC Ensembl
Innerchr4:177031925..177146627hg19UCSC Ensembl
Innerchr4:177268919..177383621hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38114703
hg19114703
hg18114703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596262
Supporting Variants
Samples
Known GenesASB5, MIR1267, SPATA4, WDR17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017028
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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