A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977896



Internal ID52660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181253091..181254413hg38UCSC Ensembl
chr5:180680091..180681413hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459095
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.205432


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