A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699939



Internal ID21221774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174114362..174114362hg38UCSC Ensembl
chr5:173541365..173541365hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699939
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.53125


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