A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34511



Internal ID12643862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34892577..34921289hg38UCSC Ensembl
Innerchr11:34914124..34942836hg19UCSC Ensembl
Innerchr11:34870700..34899412hg18UCSC Ensembl
Innerchr11:34870700..34899412hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3828713
hg1928713
hg1828713
hg1728713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6978539, essv6978538
SamplesNA11992
Known GenesAPIP, PDHX
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34511
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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