A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595754



Internal ID20968825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46780378..46781035hg38UCSC Ensembl
chr19:47283635..47284292hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245689
Samples
Known GenesSLC1A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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