A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922683



Internal ID22697908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119649333..119652480hg38UCSC Ensembl
chr11:119520043..119523190hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383148
hg193148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350020
Samples
Known GenesPVRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922683
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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