A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246674



Internal ID20813714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51744243..51745250hg38UCSC Ensembl
chr19:52247496..52248503hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381008
hg191008
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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