A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238318



Internal ID20805358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41286528..41287229hg38UCSC Ensembl
chr15:41578726..41579427hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593394
Supporting Variants
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238318
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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