A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567474



Internal ID21515811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17622519..17622575hg38UCSC Ensembl
chr2:17803786..17803842hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109842
SamplesNA20847
Known GenesVSNL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567474
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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