A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003676



Internal ID18746207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683286..109707602hg38UCSC Ensembl
Innerchr1:110225908..110250224hg19UCSC Ensembl
Innerchr1:110027431..110051747hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3824317
hg1924317
hg1824317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv265n100
Supporting Variantsnssv3701876
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)nsv1003676
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