A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056145



Internal ID21965378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3240140..3240140hg38UCSC Ensembl
chr2:3243911..3243911hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530383
Samples
Known GenesTSSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056145
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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