A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224505



Internal ID20791545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9237388..9238523hg38UCSC Ensembl
chr11:9258935..9260070hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580288
Supporting Variants
Samples
Known GenesDENND5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0007


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