A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811116



Internal ID21256454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135742958..135742958hg38UCSC Ensembl
chr5:135078647..135078647hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811116
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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