A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599603



Internal ID21548238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:980067..980495hg38UCSC Ensembl
chr11:980067..980495hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076993
SamplesHG00732
Known GenesAP2A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599603
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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