A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999144



Internal ID19158680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14585382..14691042hg38UCSC Ensembl
Innerchr3:14626889..14732549hg19UCSC Ensembl
Innerchr3:14601893..14707553hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38105661
hg19105661
hg18105661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593089
Samples
Known GenesC3orf20, CCDC174
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999144
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