A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412231



Internal ID22470101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167390725..167390725hg38UCSC Ensembl
chr4:168311876..168311876hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412231
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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