A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632925



Internal ID21581230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123881225..123881225hg38UCSC Ensembl
chr10:125640741..125640741hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066731, nssv17066732
SamplesHG00731
Known GenesCPXM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632925
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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