A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105606



Internal ID21441735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45229188..45229237hg38UCSC Ensembl
chr19:45732446..45732495hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595825
Supporting Variants
SamplesHG00732
Known GenesEXOC3L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105606
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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