A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637501



Internal ID21585806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113435379..113435379hg38UCSC Ensembl
chr10:115195138..115195138hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068338
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637501
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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