A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574521



Internal ID20947592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72732439..72735600hg38UCSC Ensembl
chr5:72028266..72031427hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg383162
hg193162
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574521
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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