A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738466



Internal ID18690061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193168634..193574329hg38UCSC Ensembl
Innerchr3:192886423..193292118hg19UCSC Ensembl
Innerchr3:194369117..194774812hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38405696
hg19405696
hg18405696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003505
Supporting Variants
Samples
Known GenesATP13A4, ATP13A5, HRASLS, MGC2889
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3738466
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