A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467280



Internal ID21124833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101050301..101051300hg38UCSC Ensembl
chr11:100921032..100922031hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985542
Samples
Known GenesPGR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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