A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106902



Internal ID21477477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9752901..9761144hg38UCSC Ensembl
chr19:9863577..9871820hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg388244
hg198244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596660
Supporting Variants
SamplesHG03486
Known GenesZNF846
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106902
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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