A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569976



Internal ID20943047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144748632..144749023hg38UCSC Ensembl
chr8:145974017..145974408hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277323
Samples
Known GenesZNF251
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569976
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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