A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013708



Internal ID18756240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109677464..109707956hg38UCSC Ensembl
Innerchr1:110220086..110250578hg19UCSC Ensembl
Innerchr1:110021609..110052101hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3830493
hg1930493
hg1830493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv265n100
Supporting Variantsnssv3494586, nssv3493031
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)nsv1013708
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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