A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568073



Internal ID20941144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102887802..102888956hg38UCSC Ensembl
chr8:103900030..103901184hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568073
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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