A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103143



Internal ID21458381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14057591..14057591hg38UCSC Ensembl
chr19:14168403..14168403hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647484
Supporting Variants
SamplesHG02587
Known GenesPALM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103143
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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