A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944841



Internal ID30564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186071444..186072094hg38UCSC Ensembl
chr3:185789233..185789883hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139394
Supporting Variants
Samples
Known GenesETV5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944841
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.011396


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