A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579787



Internal ID20952858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41316888..41317036hg38UCSC Ensembl
chr15:41609086..41609234hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238324
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579787
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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