A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029991



Internal ID18772522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183776073..183859642hg38UCSC Ensembl
Innerchr4:184697226..184780795hg19UCSC Ensembl
Innerchr4:184934220..185017789hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3883570
hg1983570
hg1883570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635609
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)nsv1029991
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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