A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944518



Internal ID30353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194433000..194791574hg38UCSC Ensembl
chr3:194153729..194512303hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38358575
hg19358575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449508
Supporting Variants
Samples
Known GenesATP13A3, FAM43A, LINC00884, LOC100507391, LSG1, TMEM44, TMEM44-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944518
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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