A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031732



Internal ID21941075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51637320..51638612hg38UCSC Ensembl
chr14:52104038..52105330hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381293
hg191293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615319
Samples
Known GenesFRMD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031732
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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