A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355224



Internal ID22580893
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 StatusS
Merged Variantsnsv5918040
Supporting Variants
Samples
Known GenesPAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355224
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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