A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240574



Internal ID20807614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90517662..90518793hg38UCSC Ensembl
chr15:91060894..91062025hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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