A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578829



Internal ID21527301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99601385..99601470hg38UCSC Ensembl
chr4:100522542..100522627hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120071
SamplesHG00171
Known GenesMTTP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578829
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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