A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887550



Internal ID22662542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11970627..11974647hg38UCSC Ensembl
chr17:11873944..11877964hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384021
hg194021
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475403, nssv17474878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887550
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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