A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2810566



Internal ID21255904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158440322..158440322hg38UCSC Ensembl
chr5:157867330..157867330hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384939
hg194939
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2810566
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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