A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704453



Internal ID21226258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51400108..51400108hg38UCSC Ensembl
chr5:50695942..50695942hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704453
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.125


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