A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055684



Internal ID21964917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238266062..238266062hg38UCSC Ensembl
chr2:239174703..239174703hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521570
Samples
Known GenesPER2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055684
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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