A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997578



Internal ID21906921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55618770..55618862hg38UCSC Ensembl
chr4:56484937..56485029hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539944
Samples
Known GenesNMU
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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