A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597183



Internal ID20970254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48255206..48256476hg38UCSC Ensembl
chr19:48758463..48759733hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381271
hg191271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246378
Samples
Known GenesCARD8, LOC100505812
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597183
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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