A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639242



Internal ID21587547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118248313..118248313hg38UCSC Ensembl
chr10:120007825..120007825hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068559, nssv17068558
SamplesHG03125, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639242
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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