A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246326



Internal ID20813366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43566255..43567919hg38UCSC Ensembl
chr19:44070407..44072071hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg381665
hg191665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597916
Supporting Variants
Samples
Known GenesXRCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246326
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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