A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579850



Internal ID21528334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23504062..23504141hg38UCSC Ensembl
chr1:23830554..23830633hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063580
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579850
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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