A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019003



Internal ID19108220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130778220..132118167hg38UCSC Ensembl
Innerchr4:131699375..133039322hg19UCSC Ensembl
Innerchr4:131918825..133258772hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381339948
hg191339948
hg181339948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639453
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)nsv1019003
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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