A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557895



Internal ID20930966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80218919..80219626hg38UCSC Ensembl
chr8:81131154..81131861hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557895
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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