A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041028



Internal ID21950364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218366474..218366474hg38UCSC Ensembl
chr2:219231197..219231197hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534060
Samples
Known GenesC2orf62
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041028
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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