A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106873



Internal ID21494206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7688879..7688942hg38UCSC Ensembl
chr19:7753765..7753828hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597446
Supporting Variants
SamplesNA19238
Known GenesFCER2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106873
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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