A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438821



Internal ID22496691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138463989..138463989hg38UCSC Ensembl
chr7:138148734..138148734hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963786
Supporting Variants
Samples
Known GenesTRIM24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438821
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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