A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567421



Internal ID20940492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67345068..68004172hg38UCSC Ensembl
chr5:66640896..67300000hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38659105
hg19659105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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