A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036021



Internal ID21945364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70425059..70425158hg38UCSC Ensembl
chr14:70891776..70891875hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036021
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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