A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627339



Internal ID21575644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113135363..113135363hg38UCSC Ensembl
chr10:114895122..114895122hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068538
SamplesHG01596
Known GenesTCF7L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627339
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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