A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742571



Internal ID20518555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3085780..3085987hg38UCSC Ensembl
chr10:3127972..3128179hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288925
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742571
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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