A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576407



Internal ID20949478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8536984..8537824hg38UCSC Ensembl
chr11:8558531..8559371hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220661
Samples
Known GenesSTK33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576407
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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