A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103019



Internal ID21428191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10377665..10377665hg38UCSC Ensembl
chr19:10488341..10488341hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650909
Supporting Variants
SamplesHG00731
Known GenesTYK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103019
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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