A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170311



Internal ID21314372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113451890..113461199hg38UCSC Ensembl
Outerchr13:113449942..113470098hg38UCSC Ensembl
Innerchr13:114106205..114115514hg19UCSC Ensembl
Outerchr13:114104257..114124413hg19UCSC Ensembl
Innerchr13:113154206..113163515hg18UCSC Ensembl
Outerchr13:113152258..113172414hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3820157
hg1920157
hg1820157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244474
SamplesNGO_23
Known GenesADPRHL1, DCUN1D2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170311
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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