A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875908



Internal ID22650867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37380839..37381892hg38UCSC Ensembl
chr17:35737777..35738830hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478215, nssv17478214
Samples
Known GenesACACA, C17orf78
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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