A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567302



Internal ID21515637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51580899..51580953hg38UCSC Ensembl
chr1:52046571..52046625hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065408
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567302
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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