A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284965



Internal ID20494183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3085780..3085780hg38UCSC Ensembl
chr10:3127972..3127972hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765403
Supporting Variants
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284965
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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