A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951987



Internal ID16954174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70043962..70061561hg38UCSC Ensembl
Outerchr15:70336301..70353900hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3817600
hg1917600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999127
SamplesBILGI_BIOE
Known GenesTLE3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951987
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