A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599811



Internal ID20972882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32853210..32853731hg38UCSC Ensembl
chr19:33344116..33344637hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245916
Samples
Known GenesSLC7A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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