A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363931



Internal ID22589600
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 StatusS
Merged Variantsnsv5923551
Supporting Variants
Samples
Known GenesDBX1, HTATIP2, NAV2, NELL1, PRMT3, SLC6A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363931
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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