A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001354



Internal ID16947620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:31535409..31660708hg38UCSC Ensembl
Outerchr3:31576901..31702200hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38125300
hg19125300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954458
Supporting Variants
SamplesBILGI_BIOE
Known GenesSTT3B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001354
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