A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437912



Internal ID216488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47217347..47222063hg38UCSC Ensembl
chr3:47258837..47263553hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384717
hg194717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932015
Samples
Known GenesKIF9-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437912
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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