A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577305



Internal ID21525756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3438033..3438100hg38UCSC Ensembl
chr2:3441804..3441871hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114017
SamplesNA19983
Known GenesTRAPPC12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577305
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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