A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953244



Internal ID17302118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:108213854..108226353hg38UCSC Ensembl
Outerchr3:107932701..107945200hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001441
SamplesBILGI_BIOE
Known GenesIFT57
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953244
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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