A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473643



Internal ID21131196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66649128..66653467hg38UCSC Ensembl
chr11:66416599..66420938hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg384340
hg194340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992580
Samples
Known GenesRBM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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