A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248375



Internal ID20815415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38769465..38793260hg38UCSC Ensembl
chr19:39260105..39283900hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823796
hg1923796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596717
Supporting Variants
Samples
Known GenesLGALS7, LGALS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248375
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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