A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811664



Internal ID21257003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2226268..2226859hg38UCSC Ensembl
chr5:2226382..2226973hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811664
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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