A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640107



Internal ID21588412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98407848..98407848hg38UCSC Ensembl
chr10:100167605..100167605hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072090
SamplesHG02587
Known GenesPYROXD2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640107
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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