A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569928



Internal ID20942999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38983567..38984990hg38UCSC Ensembl
chr5:38983669..38985092hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268317
Samples
Known GenesRICTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569928
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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