A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570802



Internal ID21519172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191758207..191758309hg38UCSC Ensembl
chr2:192622933..192623035hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110883
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570802
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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