A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722952



Internal ID146618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34574113..34667766hg38UCSC Ensembl
chr19:35065018..35158671hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3893654
hg1993654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558870
Supporting Variants
Samples
Known GenesSCGB1B2P, SCGB2B2, SCGB2B3P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722952
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.03654


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