A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556424



Internal ID21880779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122791940..122792029hg38UCSC Ensembl
chr4:123713095..123713184hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556424
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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