A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867899



Internal ID22642834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12696633..12698532hg38UCSC Ensembl
chr16:12790490..12792389hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475727
Samples
Known GenesCPPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867899
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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