A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018619



Internal ID19107836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137736635..137849866hg38UCSC Ensembl
Innerchr4:138657789..138771020hg19UCSC Ensembl
Innerchr4:138877239..138990470hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38113232
hg19113232
hg18113232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744244
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)nsv1018619
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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