A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001074



Internal ID18743605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683286..109703496hg38UCSC Ensembl
Innerchr1:110225908..110246118hg19UCSC Ensembl
Innerchr1:110027431..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3820211
hg1920211
hg1820211
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv269n100
Supporting Variantsnssv3489883, nssv3501438, nssv3484027, nssv3496269, nssv3486688, nssv3701873, nssv3701874, nssv3701875, nssv3493719, nssv3485866, nssv3490488, nssv3701872, nssv3491407, nssv3502256, nssv3499986, nssv3701871, nssv3482874
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)nsv1001074
Frequency
Sample Size29084
Observed Gain10
Observed Loss7
Observed Complex0
Frequencyn/a


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