A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596898



Internal ID20969969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35225461..35259268hg38UCSC Ensembl
chr19:35716364..35750171hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3833808
hg1933808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247644
Samples
Known GenesFAM187B, LSR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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