A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277862



Internal ID20844902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:3650292..5275479hg38UCSC Ensembl
chr8:3507814..5133001hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg381625188
hg191625188
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570855
Supporting Variants
Samples
Known GenesCSMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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