A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1656n54



Internal ID20135080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854200..11865070hg38UCSC Ensembl
chr11:11875747..11886617hg19UCSC Ensembl
chr11:11832323..11843193hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3810871
hg1910871
hg1810871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553542, nsv553541
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1656n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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