A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511667



Internal ID18463262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:198510..404317hg38UCSC Ensembl
Innerchr11:198510..404317hg19UCSC Ensembl
Innerchr11:188510..394317hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38205808
hg19205808
hg18205808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040003
Supporting Variants
Samples
Known GenesATHL1, B4GALNT4, BET1L, IFITM1, IFITM2, IFITM3, IFITM5, MIR6743, NLRP6, ODF3, PKP3, PSMD13, RIC8A, SIRT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511667
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