A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572820



Internal ID20945891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40089864..40090501hg38UCSC Ensembl
chr8:39947383..39948020hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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