A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955338



Internal ID17304211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126515258..126527557hg38UCSC Ensembl
Outerchr3:126234101..126246400hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3812300
hg1912300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001455
SamplesBILGI_BIOE
Known GenesCHST13, UROC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955338
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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