A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5464n100



Internal ID22791551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167874462..168072721hg38UCSC Ensembl
chr4:168795613..168993872hg19UCSC Ensembl
chr4:169032188..169230447hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38198260
hg19198260
hg18198260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030723, nsv1028875, nsv1016448, nsv1034450, nsv1032334, nsv1028530, nsv1021246, nsv1031538, nsv1027721, nsv1019653, nsv1032180, nsv1017771, nsv1031774, nsv1025106
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)dgv5464n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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