A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918040



Internal ID22693261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73881491..73885343hg38UCSC Ensembl
chr11:73592536..73596388hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355224
Samples
Known GenesPAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918040
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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