A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576854



Internal ID21525298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171403994..171404252hg38UCSC Ensembl
chr5:170830998..170831256hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139415
SamplesHG00732
Known GenesNPM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576854
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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