A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573634



Internal ID20946705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127811075..127816843hg38UCSC Ensembl
chr8:128823321..128829089hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg385769
hg195769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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