A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509381



Internal ID286035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18405323..18410980hg38UCSC Ensembl
chr11:18426870..18432527hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg385658
hg195658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043710
Samples
Known GenesLDHA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509381
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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