A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892350



Internal ID22667399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161074836..161075193hg38UCSC Ensembl
chr2:161931347..161931704hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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