A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433012



Internal ID22490882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138479670..138479670hg38UCSC Ensembl
chr7:138164415..138164415hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967475
Supporting Variants
Samples
Known GenesTRIM24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433012
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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