A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170020



Internal ID21314081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189447614..189452572hg38UCSC Ensembl
Outerchr3:189444582..189455007hg38UCSC Ensembl
Innerchr3:189165403..189170361hg19UCSC Ensembl
Outerchr3:189162371..189172796hg19UCSC Ensembl
Innerchr3:190648097..190653055hg18UCSC Ensembl
Outerchr3:190645065..190655490hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3810426
hg1910426
hg1810426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248071
SamplesMLY_17
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170020
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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