A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567692



Internal ID21516030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119451113..119451182hg38UCSC Ensembl
chr4:120372268..120372337hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134333
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567692
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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