A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976326



Internal ID51613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148644822..148648410hg38UCSC Ensembl
chr5:148024385..148027973hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg383589
hg193589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457238
Supporting Variants
Samples
Known GenesHTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976326
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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