A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894432



Internal ID22669504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161589973..161592847hg38UCSC Ensembl
chr2:162446483..162449357hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382875
hg192875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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