A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700979



Internal ID21222818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43343674..43343674hg38UCSC Ensembl
chr4:43345691..43345691hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700979
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.736842


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