A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038917



Internal ID21948260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39143885..39144237hg38UCSC Ensembl
chr14:39613089..39613441hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038917
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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