A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620630



Internal ID18918911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29265902..29351403hg38UCSC Ensembl
Innerchr4:29267524..29353025hg19UCSC Ensembl
Innerchr4:28876622..28962123hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3885502
hg1985502
hg1885502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008112
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)nssv3620630
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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