A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721353



Internal ID145019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10860001..10863080hg38UCSC Ensembl
chr19:10970677..10973756hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383080
hg193080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532087
Supporting Variants
Samples
Known GenesC19orf38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721353
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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