A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848735



Internal ID22623670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17186092..17187691hg38UCSC Ensembl
chr10:17228091..17229690hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451275, nssv17462496
Samples
Known GenesTRDMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848735
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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