A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278550



Internal ID20845590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67417346..67418654hg38UCSC Ensembl
chr8:68329581..68330889hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574194
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278550
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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