A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999178



Internal ID17292130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98355972..98357471hg38UCSC Ensembl
Outerchr15:98899201..98900700hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952033
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999178
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