A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007165



Internal ID18749696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109658958..109707602hg38UCSC Ensembl
Innerchr1:110201580..110250224hg19UCSC Ensembl
Innerchr1:110003103..110051747hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3848645
hg1948645
hg1848645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv257n100
Supporting Variantsnssv3492417
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)nsv1007165
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