A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449434



Internal ID227669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178739481..178739652hg38UCSC Ensembl
chr3:178457269..178457440hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942966
Samples
Known GenesKCNMB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449434
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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