A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013441



Internal ID18755972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109664687..109697544hg38UCSC Ensembl
Innerchr1:110207309..110240166hg19UCSC Ensembl
Innerchr1:110008832..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3832858
hg1932858
hg1832858
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv259n100
Supporting Variantsnssv3489205, nssv3497191
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)nsv1013441
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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