A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169615



Internal ID21313426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66880844..67216687hg38UCSC Ensembl
Innerchr9:40476154..40811997hg19UCSC Ensembl
Outerchr9:40095483..40911224hg19UCSC Ensembl
Innerchr9:40466154..40801997hg18UCSC Ensembl
Outerchr9:40085483..40901224hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38335844
hg19815742
hg18815742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244143
SamplesNGO_3
Known GenesFAM74A3, SPATA31A3, ZNF658
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169615
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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