A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888945



Internal ID22663955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13510359..13520326hg38UCSC Ensembl
chr5:13510469..13520436hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg389968
hg199968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888945
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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