A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873748



Internal ID22648696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8750296..8804400hg38UCSC Ensembl
chr16:8844153..8898257hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3854105
hg1954105
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474149
Samples
Known GenesABAT, PMM2, TMEM186
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873748
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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