A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001089



Internal ID18743620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109681750..109718120hg38UCSC Ensembl
Innerchr1:110224372..110260742hg19UCSC Ensembl
Innerchr1:110025895..110062265hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3836371
hg1936371
hg1836371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv270n100
Supporting Variantsnssv3486155
Samples
Known GenesGSTM1, GSTM2, GSTM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001089
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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