A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868893



Internal ID22643828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9090116..9105138hg38UCSC Ensembl
chr16:9183973..9198995hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3815023
hg1915023
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474818
Samples
Known GenesC16orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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