A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747469



Internal ID20523487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100807394..100807446hg38UCSC Ensembl
chr10:102567151..102567203hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258936
Samples
Known GenesPAX2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747469
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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