A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3702361



Internal ID18653956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684762..109707956hg38UCSC Ensembl
Innerchr1:110227384..110250578hg19UCSC Ensembl
Innerchr1:110028907..110052101hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3823195
hg1923195
hg1823195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012898
Supporting Variants
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3702361
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