A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479941



Internal ID22537843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10175994..10177293hg38UCSC Ensembl
chr19:10286670..10287969hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881972
Supporting Variants
Samples
Known GenesDNMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479941
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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