A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005173



Internal ID19094390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5503321..5536045hg38UCSC Ensembl
Innerchr4:5505048..5537772hg19UCSC Ensembl
Innerchr4:5555949..5588673hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3832725
hg1932725
hg1832725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616179
Samples
Known GenesC4orf6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005173
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