A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974140



Internal ID50136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142196599..142208438hg38UCSC Ensembl
chr5:141576164..141588003hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3811840
hg1911840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465849
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974140
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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