A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635570



Internal ID21583875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52006431..52006431hg38UCSC Ensembl
chr10:53766191..53766191hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070651
SamplesHG03125
Known GenesPRKG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635570
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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