A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952002



Internal ID17300876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:78038559..78077258hg38UCSC Ensembl
Outerchr15:78330901..78369600hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3838700
hg1938700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999144
SamplesBILGI_BIOE
Known GenesTBC1D2B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952002
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