A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055835



Internal ID21965068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10685916..10685916hg38UCSC Ensembl
chr2:10826042..10826042hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517771
Samples
Known GenesNOL10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055835
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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