A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021873



Internal ID21931216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40936251..41207095hg38UCSC Ensembl
chr14:41405456..41676298hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38270845
hg19270843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600920
Samples
Known GenesLOC644919
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021873
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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