A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245562



Internal ID20812602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22434951..23689752hg38UCSC Ensembl
chr19:22617753..23872554hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381254802
hg191254802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597726
Supporting Variants
Samples
Known GenesLOC100132815, LOC100996349, LOC440518, ZNF492, ZNF675, ZNF724P, ZNF728, ZNF730, ZNF91, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245562
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00059


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