A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987306



Internal ID21896649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181160359..181536468hg38UCSC Ensembl
chr2:182025086..182401195hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38376110
hg19376110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519812
Samples
Known GenesITGA4, MIR4437
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987306
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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