A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580942



Internal ID20954013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9100135..9208522hg38UCSC Ensembl
chr11:9121682..9230069hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38108388
hg19108388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231090
Samples
Known GenesDENND5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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