A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661260



Internal ID18959541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:49099237..49136966hg38UCSC Ensembl
Innerchr7:49138833..49176562hg19UCSC Ensembl
Innerchr7:49109379..49147108hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3837730
hg1937730
hg1837730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030023
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661260
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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