A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106314



Internal ID21413693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56159070..56159070hg38UCSC Ensembl
chr19:56670439..56670439hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663170
Supporting Variants
SamplesHG00513
Known GenesZNF444
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106314
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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