A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578735



Internal ID21527207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114861522..114862116hg38UCSC Ensembl
chr2:115619099..115619693hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107695
SamplesHG00171
Known GenesDPP10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578735
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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