A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7433358



Internal ID10711640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:12449829..12455950hg38UCSC Ensembl
Outerchr17:12353146..12359267hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg386122
hg196122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3163791
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7433358
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