A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468758



Internal ID21126311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62779346..62784392hg38UCSC Ensembl
chr11:62546818..62551864hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg385047
hg195047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993233
Samples
Known GenesTAF6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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