A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363495



Internal ID22589164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34150601..34152558hg38UCSC Ensembl
chr11:34172148..34174105hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381958
hg191958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918120
Supporting Variants
Samples
Known GenesABTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363495
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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