A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035098



Internal ID21944441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105990505..106572966hg38UCSC Ensembl
chr14:106456595..107028949hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38582462
hg19572355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598949
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035098
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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