A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722768



Internal ID146434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31636911..31637012hg38UCSC Ensembl
chr19:32127817..32127918hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722768
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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