A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603758



Internal ID21552424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58585599..58586555hg38UCSC Ensembl
chr20:57160655..57161611hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117153
SamplesNA19238
Known GenesAPCDD1L-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603758
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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