A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749351



Internal ID21388725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9819399..9820570hg38UCSC Ensembl
chr19:9930075..9931246hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432903
Supporting Variants
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749351
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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