A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023897



Internal ID21933240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46533182..46534730hg38UCSC Ensembl
chr14:47002385..47003933hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381549
hg191549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023897
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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