A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144249



Internal ID21420757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138313722..138313722hg38UCSC Ensembl
chr8:139325965..139325965hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624918
Supporting Variants
SamplesHG00731
Known GenesFAM135B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144249
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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