A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439116



Internal ID217661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15679828..15688503hg38UCSC Ensembl
chr2:15819952..15828627hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg388676
hg198676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909855
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439116
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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