A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354696



Internal ID22580365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1764940..1764940hg38UCSC Ensembl
chr11:1786170..1786170hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979878
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354696
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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