A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811366



Internal ID21256704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40800769..40800895hg38UCSC Ensembl
chr5:40800871..40800997hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811366
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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