A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541419



Internal ID21865774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1391148..1391148hg38UCSC Ensembl
chr4:1384936..1384936hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541419
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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