A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952302



Internal ID17301176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:19818848..19888247hg38UCSC Ensembl
Outerchr15:20024101..20093500hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3869400
hg1969400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998990
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952302
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