A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558608



Internal ID20931679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42070066..42070539hg38UCSC Ensembl
chr8:41927584..41928057hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558608
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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