A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883999



Internal ID22658981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54955565..54957064hg38UCSC Ensembl
chr17:53032926..53034425hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478837
Samples
Known GenesCOX11, TOM1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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