A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550307



Internal ID21874662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41443183..41443284hg38UCSC Ensembl
chr4:41445200..41445301hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997269
Supporting Variants
Samples
Known GenesLIMCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550307
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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