A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436685



Internal ID215295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5007119..5008765hg38UCSC Ensembl
chr3:5048804..5050450hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg381647
hg191647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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