A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244899



Internal ID20811939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21647331..22062458hg38UCSC Ensembl
chr19:21830133..22245260hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38415128
hg19415128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596360
Supporting Variants
Samples
Known GenesLOC641367, ZNF100, ZNF208, ZNF257, ZNF43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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