A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963674



Internal ID43095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8830317..8835353hg38UCSC Ensembl
chr5:8830429..8835465hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963674
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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