A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583111



Internal ID20956182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74519690..74520400hg38UCSC Ensembl
chr15:74812031..74812741hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583111
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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