A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026426



Internal ID19115644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143911121..144036829hg38UCSC Ensembl
Innerchr4:144832274..144957982hg19UCSC Ensembl
Innerchr4:145051724..145177432hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38125709
hg19125709
hg18125709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5423n100
Supporting Variantsnssv3635082
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)nsv1026426
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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