A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808687



Internal ID21254025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38081443..38081664hg38UCSC Ensembl
chr3:38122934..38123155hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678236
Samples
Known GenesDLEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808687
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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