A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571676



Internal ID21520057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46876285..46876349hg38UCSC Ensembl
chr2:47103424..47103488hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113450
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571676
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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