A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024464



Internal ID21933807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35884550..35884742hg38UCSC Ensembl
chr14:36353756..36353948hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024464
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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