A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573607



Internal ID21522013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184034159..184034209hg38UCSC Ensembl
chr3:183751947..183751997hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136888
SamplesNA19238
Known GenesHTR3D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573607
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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