A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998704



Internal ID21908047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98978978..98979197hg38UCSC Ensembl
chr4:99900129..99900348hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998704
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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