A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140202



Internal ID21486363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100461106..100461106hg38UCSC Ensembl
chr9:103223388..103223388hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633245
Supporting Variants
SamplesNA12878
Known GenesMSANTD3-TMEFF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140202
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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