A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249123



Internal ID20816163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58062179..58068709hg38UCSC Ensembl
chr19:58573547..58580077hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg386531
hg196531
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598487
Supporting Variants
Samples
Known GenesZNF135
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249123
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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