A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637085



Internal ID21829132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34537754..34750577hg38UCSC Ensembl
chr19:35028659..35241482hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38212824
hg19212824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104002
Supporting Variants
Samples
Known GenesSCGB1B2P, SCGB2B2, SCGB2B3P, ZNF181, ZNF302
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637085
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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