A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538292



Internal ID21862647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153248000..153248000hg38UCSC Ensembl
chr4:154169152..154169152hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078813
Supporting Variants
Samples
Known GenesTRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538292
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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