A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055205



Internal ID21964438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154773357..154773357hg38UCSC Ensembl
chr2:155629869..155629869hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535997
Samples
Known GenesKCNJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055205
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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