A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578776



Internal ID21527248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125204182..125204247hg38UCSC Ensembl
chr4:126125337..126125402hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128903
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578776
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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