A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426122



Internal ID22483992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119073945..119073945hg38UCSC Ensembl
chr4:119995100..119995100hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426122
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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