A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893479



Internal ID22668539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161615464..161615529hg38UCSC Ensembl
chr2:162471974..162472039hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893479
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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