A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248315



Internal ID20815355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37383559..37384317hg38UCSC Ensembl
chr19:37874461..37875219hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595627
Supporting Variants
Samples
Known GenesZNF527
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248315
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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