A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722945



Internal ID146611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34496560..34496648hg38UCSC Ensembl
chr19:34987465..34987553hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518017
Supporting Variants
Samples
Known GenesWTIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722945
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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