A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424171



Internal ID22482041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143313514..143313514hg38UCSC Ensembl
chr4:144234667..144234667hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957457
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424171
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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