A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573889



Internal ID21522297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60490972..60500361hg38UCSC Ensembl
chr1:60956644..60966033hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg389390
hg199390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067206
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573889
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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