A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693954



Internal ID21215803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42326679..42326679hg38UCSC Ensembl
chr4:42328696..42328696hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693954
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.65625


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