A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703974



Internal ID21225782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31088824..31088824hg38UCSC Ensembl
chr5:31088931..31088931hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811333
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703974
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.296875


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