A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032469



Internal ID21941812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30919321..30919376hg38UCSC Ensembl
chr14:31388527..31388582hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605010
Samples
Known GenesSTRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032469
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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