A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103112



Internal ID21493541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10182391..10182462hg38UCSC Ensembl
chr19:10293067..10293138hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598979
Supporting Variants
SamplesNA19238
Known GenesDNMT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103112
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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