A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598495



Internal ID20971566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12208918..12209445hg38UCSC Ensembl
chr19:12319733..12320260hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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