A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241929



Internal ID20808969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74211424..74212956hg38UCSC Ensembl
chr15:74503765..74505297hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241929
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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