A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572074



Internal ID21520458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9846778..9846828hg38UCSC Ensembl
chr1:9906836..9906886hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067186
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572074
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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