A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883578



Internal ID22658559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15543501..15552766hg38UCSC Ensembl
chr17:15446815..15456080hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg389266
hg199266
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475459
Samples
Known GenesTVP23C, TVP23C-CDRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883578
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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