A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565974



Internal ID20939045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132622268..132623193hg38UCSC Ensembl
chr5:131957960..131958885hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267953
Samples
Known GenesRAD50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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