A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003459



Internal ID19092677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81943670..82121819hg38UCSC Ensembl
Innerchr4:82864823..83042972hg19UCSC Ensembl
Innerchr4:83083847..83261996hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38178150
hg19178150
hg18178150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633898
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)nsv1003459
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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