A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627252



Internal ID21575557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123904876..123904876hg38UCSC Ensembl
chr10:125664392..125664392hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066734, nssv17066735
SamplesHG00731, NA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627252
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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