A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277739



Internal ID20486957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141717755..141717820hg38UCSC Ensembl
chr4:142638908..142638973hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749938
Supporting Variants
Samples
Known GenesIL15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277739
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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