A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561762



Internal ID20934833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42555826..42556902hg38UCSC Ensembl
chr8:42410969..42412045hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381077
hg191077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561762
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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