A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170029



Internal ID21314090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111396310..111410047hg38UCSC Ensembl
Outerchr13:111395049..111413363hg38UCSC Ensembl
Innerchr13:112048657..112062394hg19UCSC Ensembl
Outerchr13:112047396..112065710hg19UCSC Ensembl
Innerchr13:110846658..110860395hg18UCSC Ensembl
Outerchr13:110845397..110863711hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3818315
hg1918315
hg1818315
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242247
SamplesNGO_23
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170029
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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