A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094629



Internal ID21473672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63146250..63146250hg38UCSC Ensembl
chr15:63438449..63438449hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658582
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094629
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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