A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv261n100



Internal ID22786348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109676374..109697544hg38UCSC Ensembl
chr1:110218996..110240166hg19UCSC Ensembl
chr1:110020519..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3821171
hg1921171
hg1821171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006728, nsv1014897
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)dgv261n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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