A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv781658



Internal ID16075614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96475095..96534359hg38UCSC Ensembl
Innerchr11:96208259..96267523hg19UCSC Ensembl
Innerchr11:95847907..95907171hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3859265
hg1959265
hg1859265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555984
Supporting Variants
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv781658
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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