A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738454



Internal ID18690049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181888080..182015301hg38UCSC Ensembl
Innerchr3:181605868..181733089hg19UCSC Ensembl
Innerchr3:183088562..183215783hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38127222
hg19127222
hg18127222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005353
Supporting Variants
Samples
Known GenesLOC100996490
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3738454
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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