A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854169



Internal ID22629104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20119370..20121250hg38UCSC Ensembl
chr10:20408299..20410179hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465774
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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