A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169854



Internal ID21313665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12655485..12815096hg38UCSC Ensembl
Outerchr19:12651969..12823909hg38UCSC Ensembl
Innerchr19:12766299..12925910hg19UCSC Ensembl
Outerchr19:12762783..12934723hg19UCSC Ensembl
Innerchr19:12627299..12786910hg18UCSC Ensembl
Outerchr19:12623783..12795723hg18UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg38171941
hg19171941
hg18171941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249287
SamplesNGO_28
Known GenesASNA1, BEST2, C19orf43, DHPS, FBXW9, HOOK2, JUNB, MAN2B1, PRDX2, RNASEH2A, SNORD41, TNPO2, WDR83, WDR83OS
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169854
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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