A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995602



Internal ID21904945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122811658..122811860hg38UCSC Ensembl
chr4:123732813..123733015hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995602
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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