A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637418



Internal ID21585723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132572939..132572939hg38UCSC Ensembl
chr10:134386443..134386443hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068849
SamplesHG00732
Known GenesINPP5A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637418
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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