A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027222



Internal ID21936565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51836554..51838898hg38UCSC Ensembl
chr14:52303272..52305616hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg382345
hg192345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027222
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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