A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918571



Internal ID22693792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16866294..16866601hg38UCSC Ensembl
chr11:16887841..16888148hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357794
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918571
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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