A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001758



Internal ID18744289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109650144..109721978hg38UCSC Ensembl
Innerchr1:110192766..110264600hg19UCSC Ensembl
Innerchr1:109994289..110066123hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3871835
hg1971835
hg1871835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3501105
Samples
Known GenesGSTM1, GSTM2, GSTM4, GSTM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001758
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer