A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958002



Internal ID17306875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:100511588..100511971hg38UCSC Ensembl
Outerchr15:101051793..101052176hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005535
SamplesBILGI_BIOE
Known GenesCERS3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958002
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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