A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579135



Internal ID21527611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180860073..180860212hg38UCSC Ensembl
chr3:180577861..180578000hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125199
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579135
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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