A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170063



Internal ID21314124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:2818547..2830442hg38UCSC Ensembl
Outerchr18:2811402..2834489hg38UCSC Ensembl
Innerchr18:2818545..2830440hg19UCSC Ensembl
Outerchr18:2811400..2834487hg19UCSC Ensembl
Innerchr18:2808545..2820440hg18UCSC Ensembl
Outerchr18:2801400..2824487hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3823088
hg1923088
hg1823088
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249631
SamplesMLY_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170063
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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