A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278176



Internal ID20845216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:51386126..51386784hg38UCSC Ensembl
chr8:52298686..52299344hg19UCSC Ensembl
Cytoband8q11.22
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565005
Supporting Variants
Samples
Known GenesPXDNL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278176
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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