A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640584



Internal ID21588889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89998341..89998341hg38UCSC Ensembl
chr10:91758098..91758098hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072235, nssv17072236
SamplesHG00732, HG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640584
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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