A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643267



Internal ID18941548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20291660..20324132hg38UCSC Ensembl
Innerchr7:20331283..20363755hg19UCSC Ensembl
Innerchr7:20297808..20330280hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3832473
hg1932473
hg1832473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029085
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)nssv3643267
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