A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970621



Internal ID47739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92198429..92199866hg38UCSC Ensembl
chr5:91494246..91495683hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381438
hg191438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464308
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970621
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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