A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221461



Internal ID20788501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96029151..96032176hg38UCSC Ensembl
chr11:95762315..95765340hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383026
hg193026
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594834
Supporting Variants
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221461
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00033


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