A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275915



Internal ID20842955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101468235..101468677hg38UCSC Ensembl
chr8:102480463..102480905hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275915
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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