A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001466



Internal ID18743997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109638683..109700319hg38UCSC Ensembl
Innerchr1:110181305..110242941hg19UCSC Ensembl
Innerchr1:109982828..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3861637
hg1961637
hg1861637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv255n100
Supporting Variantsnssv3501470, nssv3489257, nssv3490949
Samples
Known GenesGSTM1, GSTM2, GSTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001466
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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