A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593394



Internal ID20966465
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 StatusM
Merged Variants
Supporting Variantsnssv18238318
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593394
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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