A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469973



Internal ID21127526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94604281..94604797hg38UCSC Ensembl
chr11:94337447..94337963hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995519
Samples
Known GenesPIWIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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