A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246672



Internal ID20813712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51718027..51718579hg38UCSC Ensembl
chr19:52221280..52221832hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596067
Supporting Variants
Samples
Known GenesHAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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