A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581151



Internal ID21529647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:103863485..103863673hg38UCSC Ensembl
chr2:104479943..104480131hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107270
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581151
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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