A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589002



Internal ID20962073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79368942..79370259hg38UCSC Ensembl
chr15:79661284..79662601hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381318
hg191318
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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