A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067593



Internal ID21403675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12198438..12198438hg38UCSC Ensembl
chr10:12240437..12240437hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642916
Supporting Variants
SamplesHG00171
Known GenesCDC123
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067593
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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