A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150968



Internal ID21503361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158701175..158701175hg38UCSC Ensembl
chr6:159122207..159122207hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643072
Supporting Variants
SamplesNA19239
Known GenesSYTL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150968
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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