A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584231



Internal ID20957302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32595295..32596373hg38UCSC Ensembl
chr11:32616841..32617919hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234585
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584231
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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