A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033855



Internal ID21943198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51832694..51838899hg38UCSC Ensembl
chr14:52299412..52305617hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg386206
hg196206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603218
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033855
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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