A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978539



Internal ID12632045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34892813..34921289hg38UCSC Ensembl
Innerchr11:34914360..34942836hg19UCSC Ensembl
Innerchr11:34870936..34899412hg18UCSC Ensembl
Innerchr11:34870936..34899412hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3828477
hg1928477
hg1828477
hg1728477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34511
Supporting Variants
SamplesNA11992
Known GenesAPIP, PDHX
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978539
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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