A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258936



Internal ID20468124
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 StatusS
Merged Variantsnsv4747469
Supporting Variants
Samples
Known GenesPAX2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16258936
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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