A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920710



Internal ID22695933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16894680..16907005hg38UCSC Ensembl
chr11:16916227..16928552hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812326
hg1912326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357785
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920710
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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