A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577034



Internal ID20950105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115732578..115742708hg38UCSC Ensembl
chr11:115603296..115613426hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3810131
hg1910131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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