A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682062



Internal ID21203920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3293813..3293813hg38UCSC Ensembl
chr4:3295540..3295540hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682062
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.232143


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