A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239674



Internal ID20806714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76371401..76371812hg38UCSC Ensembl
chr15:76663742..76664153hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589761
Supporting Variants
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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