A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882385



Internal ID22657362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5780827..5781919hg38UCSC Ensembl
chr17:5684147..5685239hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475153
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882385
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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