A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922775



Internal ID22698000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37974554..37986845hg38UCSC Ensembl
chr11:37996104..38008395hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3812292
hg1912292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922775
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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