A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170059



Internal ID21314120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79404842..79422231hg38UCSC Ensembl
Outerchr1:79404507..79424100hg38UCSC Ensembl
Innerchr1:79870527..79887916hg19UCSC Ensembl
Outerchr1:79870192..79889785hg19UCSC Ensembl
Innerchr1:79643115..79660504hg18UCSC Ensembl
Outerchr1:79642780..79662373hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3819594
hg1919594
hg1819594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242582
SamplesNGO_12
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170059
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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