A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572872



Internal ID20945943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22958825..22959302hg38UCSC Ensembl
chr8:22816338..22816815hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572872
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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