A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566049



Internal ID20939120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83119140..83126053hg38UCSC Ensembl
chr5:82414959..82421872hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg386914
hg196914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269635
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566049
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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