A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887290



Internal ID22662282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48487992..48489260hg38UCSC Ensembl
chr17:46565354..46566622hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381269
hg191269
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887290
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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