A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5961n100



Internal ID20157577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52748106..52827956hg38UCSC Ensembl
chr6:52612904..52692754hg19UCSC Ensembl
chr6:52720863..52800713hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3879851
hg1979851
hg1879851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016274, nsv1030141
Samples
Known GenesGSTA1, GSTA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5961n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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