A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568050



Internal ID20941121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93630785..93631040hg38UCSC Ensembl
chr5:92966491..92966746hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267702
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568050
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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