A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5429n100



Internal ID22791516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143988099..144038174hg38UCSC Ensembl
chr4:144909252..144959327hg19UCSC Ensembl
chr4:145128702..145178777hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3850076
hg1950076
hg1850076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024570, nsv1030769, nsv1018549, nsv1029199
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)dgv5429n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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