A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091722



Internal ID21484087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66509831..66509831hg38UCSC Ensembl
chr15:66802169..66802169hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647435
Supporting Variants
SamplesNA12329
Known GenesZWILCH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091722
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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