A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016258



Internal ID19105477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144003421..144098631hg38UCSC Ensembl
Innerchr4:144924574..145019784hg19UCSC Ensembl
Innerchr4:145144024..145239234hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3895211
hg1995211
hg1895211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5428n100
Supporting Variantsnssv3636036
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)nsv1016258
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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