A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811146



Internal ID21256484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151166575..151166575hg38UCSC Ensembl
chr5:150546136..150546136hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382473
hg192473
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811146
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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