A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554308



Internal ID21878663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177045909..177229534hg38UCSC Ensembl
chr4:177967063..178150688hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38183626
hg19183626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554308
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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