A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094169



Internal ID21431342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80911950..80911950hg38UCSC Ensembl
chr15:81204291..81204291hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646858
Supporting Variants
SamplesHG00731
Known GenesKIAA1199
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094169
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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