A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578996



Internal ID21527471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127854828..127857381hg38UCSC Ensembl
chr4:128775983..128778536hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg382554
hg192554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135254
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578996
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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