A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572219



Internal ID20945290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60979469..60980770hg38UCSC Ensembl
chr8:61892028..61893329hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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