A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278397



Internal ID20845437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61693566..61693813hg38UCSC Ensembl
chr8:62606125..62606372hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563555
Supporting Variants
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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