A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988311



Internal ID12634567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130263320..130329843hg38UCSC Ensembl
Innerchr11:130133215..130199738hg19UCSC Ensembl
Innerchr11:129638425..129704948hg18UCSC Ensembl
Innerchr11:129638425..129704948hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3866524
hg1966524
hg1866524
hg1766524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34550
Supporting Variants
SamplesNA18952
Known GenesZBTB44
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988311
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