A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519132



Internal ID18817413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31600987..31673444hg38UCSC Ensembl
Innerchr11:31622534..31694992hg19UCSC Ensembl
Innerchr11:31579110..31651568hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3872458
hg1972459
hg1872459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052305
Supporting Variants
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519132
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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