A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169684



Internal ID21313495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27418968..28031820hg38UCSC Ensembl
Outerchr19:27390278..28038503hg38UCSC Ensembl
Innerchr19:27909876..28522727hg19UCSC Ensembl
Outerchr19:27881186..28529410hg19UCSC Ensembl
Innerchr19:32601716..33214567hg18UCSC Ensembl
Outerchr19:32573026..33221250hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38648226
hg19648225
hg18648225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249434
SamplesMLY_8
Known GenesLINC00662
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169684
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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