A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587634



Internal ID20960705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17486836..17489258hg38UCSC Ensembl
chr11:17508383..17510805hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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