A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv274n100



Internal ID20151890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109690340..109703496hg38UCSC Ensembl
chr1:110232962..110246118hg19UCSC Ensembl
chr1:110034485..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3813157
hg1913157
hg1813157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005251, nsv999409
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)dgv274n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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