A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578995



Internal ID21527470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46876263..46876457hg38UCSC Ensembl
chr2:47103402..47103596hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113449
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578995
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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