A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811563



Internal ID21256902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16624233..16624304hg38UCSC Ensembl
chr5:16624342..16624413hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811563
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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