A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585357



Internal ID20958428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75393112..75393562hg38UCSC Ensembl
chr15:75685453..75685903hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241970
Samples
Known GenesSIN3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585357
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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