A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997751



Internal ID21907094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56723174..56792272hg38UCSC Ensembl
chr4:57589340..57658438hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3869099
hg1969099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997751
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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