A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996202



Internal ID21905545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155018434..155021441hg38UCSC Ensembl
chr4:155939586..155942593hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg383008
hg193008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996202
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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