A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460090



Internal ID21117643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121075501..121078000hg38UCSC Ensembl
chr11:120946210..120948709hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986846
Samples
Known GenesTBCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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