A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869282



Internal ID22644217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23859459..23859590hg38UCSC Ensembl
chr2:24082329..24082460hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397418
Samples
Known GenesATAD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869282
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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