A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597209



Internal ID20970280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9088902..9089441hg38UCSC Ensembl
chr19:9199578..9200117hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597209
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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