A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17349817



Internal ID22575557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32809557..32815136hg38UCSC Ensembl
chr11:32831103..32836682hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385580
hg195580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17349817
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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