A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854662



Internal ID22629597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47380667..47384852hg38UCSC Ensembl
chr10:48354510..48358695hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg384186
hg194186
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463489
Samples
Known GenesZNF488
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854662
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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