A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923551



Internal ID22698778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20096010..20731492hg38UCSC Ensembl
chr11:20117556..20753038hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38635483
hg19635483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363931
Samples
Known GenesDBX1, HTATIP2, NAV2, NELL1, PRMT3, SLC6A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923551
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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