A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586822



Internal ID20959893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59615251..60468567hg38UCSC Ensembl
chr15:59907450..60760766hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38853317
hg19853317
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241215
Samples
Known GenesANXA2, BNIP2, FOXB1, GCNT3, GTF2A2, NARG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586822
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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