A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169379



Internal ID21313862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10739058..10764097hg38UCSC Ensembl
Outerchr9:10737968..10770064hg38UCSC Ensembl
Innerchr9:10739058..10764097hg19UCSC Ensembl
Outerchr9:10737968..10770064hg19UCSC Ensembl
Innerchr9:10729058..10754097hg18UCSC Ensembl
Outerchr9:10727968..10760064hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3832097
hg1932097
hg1832097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247581, nssv14251507, nssv14244556, nssv14243332
SamplesSNI_2, SNI_10, NGO_32, NGO_11
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169379
Frequency
Sample Size93
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer