A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575470



Internal ID21523899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86985383..86985434hg38UCSC Ensembl
chr1:87451066..87451117hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067060
SamplesHG02011
Known GenesHS2ST1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575470
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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