A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581978



Internal ID20955049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28129586..28130146hg38UCSC Ensembl
chr11:28151133..28151693hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224856
Samples
Known GenesMETTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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