A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806803



Internal ID21252141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13450019..13450019hg38UCSC Ensembl
chr3:13491519..13491519hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806803
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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