A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982087



Internal ID12974422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97165990..97213990hg38UCSC Ensembl
Innerchr11:97036990..97084990hg19UCSC Ensembl
Innerchr11:96542200..96590200hg18UCSC Ensembl
Innerchr11:96542200..96590200hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3848001
hg1948001
hg1848001
hg1748001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751037
Supporting Variants
SamplesBEC_519
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982087
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