A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884929



Internal ID22659913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50318571..50323670hg38UCSC Ensembl
chr17:48395932..48401031hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475056, nssv17478825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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