A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976831



Internal ID51941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177683324..177739324hg38UCSC Ensembl
chr5:177110325..177166325hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3856001
hg1956001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455135
Supporting Variants
Samples
Known GenesFAM153A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976831
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008281


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