A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030821



Internal ID21940164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81011580..81016814hg38UCSC Ensembl
chr14:81477924..81483158hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg385235
hg195235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603274
Samples
Known GenesTSHR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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