A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238094



Internal ID20805134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50358263..50359606hg38UCSC Ensembl
chr15:50650460..50651803hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381344
hg191344
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581889
Supporting Variants
Samples
Known GenesGABPB1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238094
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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