A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634159



Internal ID21582464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83955153..83955153hg38UCSC Ensembl
chr10:85714909..85714909hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071917, nssv17071918
SamplesHG00512, NA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634159
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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