A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170096



Internal ID21314157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1280588..1334748hg38UCSC Ensembl
Outerchr19:1272041..1337377hg38UCSC Ensembl
Innerchr19:1280587..1334747hg19UCSC Ensembl
Outerchr19:1272040..1337376hg19UCSC Ensembl
Innerchr19:1231587..1285747hg18UCSC Ensembl
Outerchr19:1223040..1288376hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3865337
hg1965337
hg1865337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244874
SamplesMLY_12
Known GenesC19orf24, CIRBP, EFNA2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170096
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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