A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583404



Internal ID20956475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74901741..74904342hg38UCSC Ensembl
chr15:75194082..75196683hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241951
Samples
Known GenesFAM219B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583404
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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