A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv265n100



Internal ID19010633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109677464..109714002hg38UCSC Ensembl
chr1:110220086..110256624hg19UCSC Ensembl
chr1:110021609..110058147hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3836539
hg1936539
hg1836539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997290, nsv1014454, nsv1006594, nsv1001347, nsv1000643, nsv1006811, nsv1001491, nsv1000819, nsv1005194, nsv1012898, nsv1007916, nsv1003676, nsv1013708, nsv1010244, nsv998938
Samples
Known GenesGSTM1, GSTM2, GSTM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv265n100
Frequency
Sample Size29084
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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