A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809820



Internal ID21255158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174038101..174038101hg38UCSC Ensembl
chr4:174959252..174959252hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809820
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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