A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590998



Internal ID20964069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76120545..76121417hg38UCSC Ensembl
chr15:76412886..76413758hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242007
Samples
Known GenesC15orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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