A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435353



Internal ID214004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137395898..137397891hg38UCSC Ensembl
chr3:137114740..137116733hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381994
hg191994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435353
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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