A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1411513



Internal ID12227949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907658..89907707hg38UCSC Ensembl
chr16:89974066..89974115hg19UCSC Ensembl
chr16:88501567..88501616hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3733394
SamplesHuRef
Known GenesTCF25
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1411513
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