A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578864



Internal ID21527337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66445172..66445231hg38UCSC Ensembl
chr1:66910855..66910914hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066380
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578864
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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