A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887338



Internal ID22662330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75411579..75414153hg38UCSC Ensembl
chr17:73407660..73410234hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382575
hg192575
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887338
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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