A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967948



Internal ID22742883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22806402..23350599hg38UCSC Ensembl
chr19:22989204..23533401hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38544198
hg19544198
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401498
Samples
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967948
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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