A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739766



Internal ID20515741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81383463..81384522hg38UCSC Ensembl
chr14:81849807..81850866hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258969
Samples
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739766
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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