A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908364



Internal ID22683574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124929697..124930024hg38UCSC Ensembl
chr11:124799593..124799920hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363252
Samples
Known GenesHEPACAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908364
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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