A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241959



Internal ID20808999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75225241..75762978hg38UCSC Ensembl
chr15:75517582..76055319hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38537738
hg19537738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588320
Supporting Variants
Samples
Known GenesCOMMD4, CSPG4, DNM1P35, GOLGA6C, GOLGA6D, IMP3, MAN2C1, MIR4313, MIR631, NEIL1, ODF3L1, PTPN9, SIN3A, SNUPN, SNX33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241959
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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