A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980653



Internal ID12971771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97835738..97896017hg38UCSC Ensembl
Innerchr11:97706738..97767017hg19UCSC Ensembl
Innerchr11:97211948..97272227hg18UCSC Ensembl
Innerchr11:97211948..97272227hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3860280
hg1960280
hg1860280
hg1760280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751038
Supporting Variants
SamplesBEC_101
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980653
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