A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105246



Internal ID21464214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43610531..43610531hg38UCSC Ensembl
chr19:44114683..44114683hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653574
Supporting Variants
SamplesHG03065
Known GenesZNF428
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105246
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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