A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2106n54



Internal ID22770001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96475095..96542845hg38UCSC Ensembl
chr11:96208259..96276010hg19UCSC Ensembl
chr11:95847907..95915658hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3867751
hg1967752
hg1867752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555986, nsv555984, nsv555985
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2106n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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