A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704811



Internal ID21226615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168755390..168755390hg38UCSC Ensembl
chr5:168182395..168182395hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812002
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704811
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.103448


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