A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573875



Internal ID21522283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26644925..26645006hg38UCSC Ensembl
chr4:26646547..26646628hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136189
SamplesHG03486
Known GenesTBC1D19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573875
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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