A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv275n100



Internal ID22786362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109690340..109710508hg38UCSC Ensembl
chr1:110232962..110253130hg19UCSC Ensembl
chr1:110034485..110054653hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3820169
hg1920169
hg1820169
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010810, nsv1001968, nsv998493, nsv999912, nsv1014873
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv275n100
Frequency
Sample Size11257
Observed Gain23
Observed Loss39
Observed Complex0
Frequencyn/a


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