A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584935



Internal ID20958006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71952691..71953211hg38UCSC Ensembl
chr11:71663737..71664257hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225799
Samples
Known GenesRNF121
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584935
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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