A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982788



Internal ID12628853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:242317308..242730382hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17413075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751857
Supporting Variants
SamplesBEC_593
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982788
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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