A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763033



Internal ID16056989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:174837..196533hg38UCSC Ensembl
Innerchr11:174837..196533hg19UCSC Ensembl
Innerchr11:164837..186533hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3821697
hg1921697
hg1821697
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552758
Supporting Variants
Samples
Known GenesLOC653486, SCGB1C1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763033
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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