A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750659



Internal ID21388020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8104523..8104888hg38UCSC Ensembl
chr19:8169407..8169772hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432889
Supporting Variants
SamplesNB07
Known GenesFBN3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750659
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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