A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508004



Internal ID284706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38545828..38606832hg38UCSC Ensembl
chr13:39119965..39180969hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3861005
hg1961005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686999
Samples
Known GenesLINC00366
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508004
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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