A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067650



Internal ID21435205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125824766..125824766hg38UCSC Ensembl
chr10:127513335..127513335hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639815
Supporting Variants
SamplesHG00731
Known GenesBCCIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067650
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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