A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625686



Internal ID21573991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59225143..59225143hg38UCSC Ensembl
chr10:60984903..60984903hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071080
SamplesHG00731
Known GenesPHYHIPL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625686
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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