A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997188



Internal ID21906531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38999171..38999223hg38UCSC Ensembl
chr4:39000791..39000843hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549135
Samples
Known GenesTMEM156
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997188
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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