A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998014



Internal ID21907357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56769910..56771225hg38UCSC Ensembl
chr4:57636076..57637391hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998014
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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