A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169460



Internal ID21313943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:64688996..64712980hg38UCSC Ensembl
Outerchr8:64682360..64717398hg38UCSC Ensembl
Innerchr8:65601553..65625537hg19UCSC Ensembl
Outerchr8:65594917..65629955hg19UCSC Ensembl
Innerchr8:65764107..65788091hg18UCSC Ensembl
Outerchr8:65757471..65792509hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3835039
hg1935039
hg1835039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14240868
SamplesSNI_9
Known GenesCYP7B1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169460
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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