A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358061



Internal ID22583730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65025779..65025779hg38UCSC Ensembl
chr11:64793251..64793251hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973609
Supporting Variants
Samples
Known GenesARL2-SNX15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358061
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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