A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638224



Internal ID21586529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6283540..6283540hg38UCSC Ensembl
chr10:6325503..6325503hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070456
SamplesHG03371
Known GenesLOC399715
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638224
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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