A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581938



Internal ID20955009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125601350..125601849hg38UCSC Ensembl
chr11:125471245..125471744hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218072
Samples
Known GenesSTT3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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