A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975835



Internal ID51288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155266880..155267176hg38UCSC Ensembl
chr5:154646440..154646736hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461637
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975835
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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