A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900209



Internal ID22675349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163074949..163081034hg38UCSC Ensembl
chr2:163931459..163937544hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg386086
hg196086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900209
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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