A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988818



Internal ID12630486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21072035..22777875hg19UCSC Ensembl
Innerchr15:19336725..20329239hg18UCSC Ensembl
Innerchr15:19336725..20329239hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg191705841
hg18992515
hg17992515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751354
Supporting Variants
SamplesBEC_718
Known GenesCT60, CXADRP2, GOLGA6L1, GOLGA8DP, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988818
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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