A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv267n100



Internal ID22786354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109681750..109697544hg38UCSC Ensembl
chr1:110224372..110240166hg19UCSC Ensembl
chr1:110025895..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3815795
hg1915795
hg1815795
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006502, nsv1010592, nsv1008891, nsv1013811, nsv1004988, nsv1006939, nsv999907, nsv1014059, nsv1013492, nsv1012344
Samples
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv267n100
Frequency
Sample Size11257
Observed Gain255
Observed Loss356
Observed Complex0
Frequencyn/a


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