A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4198309



Internal ID11480847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28193..28265hg38UCSC Ensembl
chr9:28193..28265hg19UCSC Ensembl
chr9:18193..18265hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3873
hg1973
hg1873
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1199599
Supporting Variants
SamplesHuRef
Known GenesWASH1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4198309
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