A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939842



Internal ID22715241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8342887..8344667hg38UCSC Ensembl
chr17:8246205..8247985hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381781
hg191781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv879n209
Supporting Variantsnssv17371378
Samples
Known GenesODF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939842
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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