A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585901



Internal ID20958972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98275519..100478499hg38UCSC Ensembl
chr11:98146247..100349230hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382202981
hg192202984
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221094
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585901
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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