A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169360



Internal ID21313843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92109768..92120266hg38UCSC Ensembl
Outerchr15:92109106..92121834hg38UCSC Ensembl
Innerchr15:92652998..92663496hg19UCSC Ensembl
Outerchr15:92652336..92665064hg19UCSC Ensembl
Innerchr15:90454002..90464500hg18UCSC Ensembl
Outerchr15:90453340..90466068hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812729
hg1912729
hg1812729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244558
SamplesNGO_24
Known GenesSLCO3A1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169360
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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