A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170106



Internal ID21314167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145274083..145333029hg38UCSC Ensembl
Outerchr3:145272256..145337029hg38UCSC Ensembl
Innerchr3:144991870..145050816hg19UCSC Ensembl
Outerchr3:144990043..145054816hg19UCSC Ensembl
Innerchr3:146474560..146533506hg18UCSC Ensembl
Outerchr3:146472733..146537506hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3864774
hg1964774
hg1864774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246327
SamplesNGO_18
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170106
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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