A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587064



Internal ID20960135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83417408..83423719hg38UCSC Ensembl
chr15:84086160..84092471hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386312
hg196312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587064
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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