A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5963n100



Internal ID22792050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52767793..52808133hg38UCSC Ensembl
chr6:52632591..52672931hg19UCSC Ensembl
chr6:52740550..52780890hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3840341
hg1940341
hg1840341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027144, nsv1028837, nsv1033017
Samples
Known GenesGSTA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5963n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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