A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3908889



Internal ID11852982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28821815..28822477hg38UCSC Ensembl
chr17:27148833..27149495hg19UCSC Ensembl
chr17:24172959..24173621hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38663
hg19663
hg18663
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1280050
Supporting Variants
SamplesHuRef
Known GenesFAM222B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3908889
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