A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594609



Internal ID20967680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112053088..112053654hg38UCSC Ensembl
chr11:111923812..111924378hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221385
Samples
Known GenesDLAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594609
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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