A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567138



Internal ID21515470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1828362..1828627hg38UCSC Ensembl
chr4:1830089..1830354hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129614
SamplesNA19238
Known GenesLETM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567138
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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