A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279167



Internal ID20846207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95760239..95762230hg38UCSC Ensembl
chr8:96772467..96774458hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381992
hg191992
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569970
Supporting Variants
Samples
Known GenesLOC100616530
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279167
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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