A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106265



Internal ID21401422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55097586..55097586hg38UCSC Ensembl
chr19:55608954..55608954hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651852
Supporting Variants
SamplesHG00096
Known GenesPPP1R12C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106265
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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