A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021007



Internal ID21930350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104922185..104922662hg38UCSC Ensembl
chr14:105388522..105388999hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021007
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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