A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873666



Internal ID22648614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23113272..23131828hg38UCSC Ensembl
chr2:23336143..23354699hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3818557
hg1918557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873666
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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