A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436500



Internal ID215114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108126929..108127048hg38UCSC Ensembl
chr3:107845776..107845895hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436500
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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