A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625222



Internal ID21573527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29938900..29938900hg38UCSC Ensembl
chr10:30227829..30227829hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070338
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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