A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003914



Internal ID18746445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684109..109741677hg38UCSC Ensembl
Innerchr1:110226731..110284299hg19UCSC Ensembl
Innerchr1:110028254..110085822hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3857569
hg1957569
hg1857569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3485947
Samples
Known GenesGSTM1, GSTM3, GSTM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003914
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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