A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083950



Internal ID21993183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50015889..50015889hg38UCSC Ensembl
chr14:50482607..50482607hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600250
Samples
Known GenesLOC100506499
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083950
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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