A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922220



Internal ID22697445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3495175..3643117hg38UCSC Ensembl
chr11:3516405..3664347hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38147943
hg19147943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363290
Samples
Known GenesART5, TRPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922220
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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