A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543644



Internal ID21867999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4348554..4348657hg38UCSC Ensembl
chr4:4350281..4350384hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543644
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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