A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625100



Internal ID18923381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44964987..45004163hg38UCSC Ensembl
Innerchr4:44967004..45006180hg19UCSC Ensembl
Innerchr4:44661761..44700937hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3839177
hg1939177
hg1839177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007329
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)nssv3625100
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