A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643412



Internal ID21591717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116633652..116633652hg38UCSC Ensembl
chr10:118393163..118393163hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067552
SamplesHG00731
Known GenesPNLIPRP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643412
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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