A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148903



Internal ID21482992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26874085..26874085hg38UCSC Ensembl
chr6:26841864..26841864hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636342
Supporting Variants
SamplesHG03732
Known GenesGUSBP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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