A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594062



Internal ID20967133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69189029..69194767hg38UCSC Ensembl
chr11:68956497..68962234hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385739
hg195738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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