A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976001



Internal ID51401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160178237..160179808hg38UCSC Ensembl
chr5:159605244..159606815hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381572
hg191572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976001
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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