A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032137



Internal ID21941480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35936710..35951721hg38UCSC Ensembl
chr14:36405916..36420927hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3815012
hg1915012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032137
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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