A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103421



Internal ID21442922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1967786..1967975hg38UCSC Ensembl
chr19:1967785..1967974hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593845
Supporting Variants
SamplesHG00732
Known GenesCSNK1G2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103421
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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