A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277076



Internal ID20844116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119581008..119582008hg38UCSC Ensembl
chr8:120593248..120594248hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575067
Supporting Variants
Samples
Known GenesENPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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