A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240586



Internal ID20807626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90721370..90721883hg38UCSC Ensembl
chr15:91264601..91265114hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588530
Supporting Variants
Samples
Known GenesBLM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240586
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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