A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1004465



Internal ID16298421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114025712..114334122hg38UCSC Ensembl
Innerchr4:114946868..115255278hg19UCSC Ensembl
Innerchr4:115166317..115474727hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38308411
hg19308411
hg18308411
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595184
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1004465
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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