A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16972477



Internal ID49005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99036585..99040547hg38UCSC Ensembl
chr5:98372289..98376251hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg383963
hg193963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16972477
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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