A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv52n137



Internal ID22812672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128585004..128585095hg38UCSC Ensembl
chr11:128454899..128454990hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2789540, nsv2789889
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv52n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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