A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242533



Internal ID21307177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5510228..5513051hg38UCSC Ensembl
Outerchr19:5506648..5515782hg38UCSC Ensembl
Innerchr19:5510239..5513062hg19UCSC Ensembl
Outerchr19:5506659..5515793hg19UCSC Ensembl
Innerchr19:5461239..5464062hg18UCSC Ensembl
Outerchr19:5457659..5466793hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389135
hg199135
hg189135
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170039
Supporting Variants
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242533
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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