A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632151



Internal ID21580456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122200942..122200942hg38UCSC Ensembl
chr10:123960457..123960457hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067598
SamplesHG03009
Known GenesTACC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632151
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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