A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060277



Internal ID21969511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239085860..239085860hg38UCSC Ensembl
chr2:240007556..240007556hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533758
Samples
Known GenesHDAC4, MIR4441
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060277
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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