A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878783



Internal ID22653748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4775181..4790868hg38UCSC Ensembl
chr17:4678476..4694163hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3815688
hg1915688
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478816
Samples
Known GenesGLTPD2, TM4SF5, VMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878783
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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