A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466920



Internal ID21124473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63956744..63959284hg38UCSC Ensembl
chr11:63724216..63726756hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382541
hg192541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993822
Samples
Known GenesNAA40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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