A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149078



Internal ID21481073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38396604..38396604hg38UCSC Ensembl
chr8:38254122..38254122hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629069
Supporting Variants
SamplesHG03683
Known GenesLETM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149078
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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