A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125795



Internal ID21414935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153247983..153247983hg38UCSC Ensembl
chr4:154169135..154169135hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618128
Supporting Variants
SamplesHG00513
Known GenesTRIM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125795
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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