A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580130



Internal ID20953201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118621181..118624038hg38UCSC Ensembl
chr11:118491896..118494755hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382858
hg192860
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233056
Samples
Known GenesPHLDB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580130
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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