A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461879



Internal ID239822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161316369..161317148hg38UCSC Ensembl
chr5:160743376..160744155hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977460
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461879
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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