A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999373



Internal ID17292325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:15884603..15892102hg38UCSC Ensembl
Outerchr9:15884601..15892100hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950842
Supporting Variants
SamplesBILGI_BIOE
Known GenesCCDC171
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999373
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