A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569579



Internal ID20942650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140665394..140665972hg38UCSC Ensembl
chr5:140044979..140045557hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267507
Samples
Known GenesWDR55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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