A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407996



Internal ID22465866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34537657..34749386hg38UCSC Ensembl
chr19:35028562..35240291hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38211730
hg19211730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975015
Supporting Variants
Samples
Known GenesSCGB1B2P, SCGB2B2, SCGB2B3P, ZNF181, ZNF302
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407996
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer