A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928082



Internal ID22703317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4763992..4780332hg38UCSC Ensembl
chr17:4667287..4683627hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3816341
hg1916341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383040
Samples
Known GenesTM4SF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928082
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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