A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv259n100



Internal ID20151875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109663341..109700319hg38UCSC Ensembl
chr1:110205963..110242941hg19UCSC Ensembl
chr1:110007486..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3836979
hg1936979
hg1836979
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011258, nsv1013441
Samples
Known GenesGSTM1, GSTM2, GSTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv259n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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