A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010843



Internal ID19100060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34062631..34207220hg38UCSC Ensembl
Innerchr4:34064253..34208842hg19UCSC Ensembl
Innerchr4:33740648..33885237hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38144590
hg19144590
hg18144590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620654
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010843
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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