A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808443



Internal ID21253781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151558007..151558007hg38UCSC Ensembl
chr3:151275795..151275795hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808443
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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