A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586724



Internal ID20959795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26103082..26104066hg38UCSC Ensembl
chr11:26124629..26125613hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586724
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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