A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051409



Internal ID21960642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224776317..224776317hg38UCSC Ensembl
chr2:225641034..225641034hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537503
Samples
Known GenesDOCK10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051409
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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