A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401498



Internal ID22459368
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 StatusS
Merged Variantsnsv5967948
Supporting Variants
Samples
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401498
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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