A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880476



Internal ID22655446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58585567..58586566hg38UCSC Ensembl
chr20:57160623..57161622hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486734
Samples
Known GenesAPCDD1L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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