A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288925



Internal ID20498143
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 StatusS
Merged Variantsnsv4742571
Supporting Variants
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288925
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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