A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867893



Internal ID22642828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44663480..44665954hg38UCSC Ensembl
chr17:42740848..42743322hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474384
Samples
Known GenesC17orf104
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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