A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007399



Internal ID18749930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109691597..109726206hg38UCSC Ensembl
Innerchr1:110234219..110268828hg19UCSC Ensembl
Innerchr1:110035742..110070351hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3834610
hg1934610
hg1834610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492669
Samples
Known GenesGSTM1, GSTM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007399
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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