A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936139



Internal ID24808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77763670..77769678hg38UCSC Ensembl
chr3:77812821..77818829hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg386009
hg196009
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147133
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936139
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.033874


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