A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509802



Internal ID286445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119183895..119191538hg38UCSC Ensembl
chr10:120943407..120951050hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg387644
hg197644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n206
Supporting Variantsnssv17040866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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