A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883022



Internal ID22657999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6667918..6672117hg38UCSC Ensembl
chr17:6571237..6575436hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883022
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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