A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1168353



Internal ID11984790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15104470..15104541hg38UCSC Ensembl
chr16:15198327..15198398hg19UCSC Ensembl
chr16:15105828..15105899hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4248744
SamplesHuRef
Known GenesPDXDC1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1168353
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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