A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975015



Internal ID22749950
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 StatusM
Merged Variants
Supporting Variantsnssv17407996
Samples
Known GenesSCGB1B2P, SCGB2B2, SCGB2B3P, ZNF181, ZNF302
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975015
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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