A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276184



Internal ID20843224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125353647..125354239hg38UCSC Ensembl
chr8:126365889..126366481hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566394
Supporting Variants
Samples
Known GenesNSMCE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276184
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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