A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590849



Internal ID20963920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75228822..75230279hg38UCSC Ensembl
chr15:75521163..75522620hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590849
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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