A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710079



Internal ID18661674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34620051..34772477hg38UCSC Ensembl
Innerchr11:34641598..34794024hg19UCSC Ensembl
Innerchr11:34598174..34750600hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38152427
hg19152427
hg18152427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052008
Supporting Variants
Samples
Known GenesEHF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710079
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