A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148955



Internal ID21449589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39906030..39906030hg38UCSC Ensembl
chr6:39873806..39873806hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636112
Supporting Variants
SamplesHG01114
Known GenesMOCS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148955
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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