A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722683



Internal ID146349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29966301..29973567hg38UCSC Ensembl
chr19:30457208..30464474hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg387267
hg197267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522552
Supporting Variants
Samples
Known GenesURI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722683
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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