A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589031



Internal ID20962102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39446132..39446900hg38UCSC Ensembl
chr15:39738333..39739101hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589031
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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