A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568402



Internal ID20941473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70617892..70618481hg38UCSC Ensembl
chr8:71530127..71530716hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278632
Samples
Known GenesLOC286190
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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