A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878352



Internal ID22653317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83195506..83199371hg38UCSC Ensembl
chr17:81143275..81147140hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383866
hg193866
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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