A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593581



Internal ID20966652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34636878..34638076hg38UCSC Ensembl
chr11:34658425..34659623hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232696
Samples
Known GenesEHF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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