A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952893



Internal ID17301767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:101953898..101969997hg38UCSC Ensembl
Outerchr15:102494101..102510200hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3816100
hg1916100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999188
SamplesBILGI_BIOE
Known GenesFAM138E, WASH3P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952893
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