A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv268n100



Internal ID22786355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109681750..109700319hg38UCSC Ensembl
chr1:110224372..110242941hg19UCSC Ensembl
chr1:110025895..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3818570
hg1918570
hg1818570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012161, nsv1004059, nsv1007317, nsv1013410, nsv1010298, nsv998013, nsv999820
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)dgv268n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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