A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030457



Internal ID18772988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143920939..144107278hg38UCSC Ensembl
Innerchr4:144842092..145028431hg19UCSC Ensembl
Innerchr4:145061542..145247881hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38186340
hg19186340
hg18186340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5421n100
Supporting Variantsnssv3635228
Samples
Known GenesGYPB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030457
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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