A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905902



Internal ID22681095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:120183031..120183114hg38UCSC Ensembl
chr2:120940607..120940690hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905902
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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