A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538946



Internal ID21863301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57993152..57993152hg38UCSC Ensembl
chr4:58859318..58859318hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538946
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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