A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572555



Internal ID20945626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98109085..98109763hg38UCSC Ensembl
chr8:99121313..99121991hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279227
Samples
Known GenesHRSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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