A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590424



Internal ID20963495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95860915..95861447hg38UCSC Ensembl
chr11:95594079..95594611hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221578
Samples
Known GenesMTMR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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