A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450348



Internal ID21107901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16894680..16907006hg38UCSC Ensembl
chr11:16916227..16928553hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812327
hg1912327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988736
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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