A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983883



Internal ID12630644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22032085..22181985hg38UCSC Ensembl
Innerchr15:22320036..22469936hg19UCSC Ensembl
Innerchr15:19821400..19971300hg18UCSC Ensembl
Innerchr15:19821400..19971300hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38149901
hg19149901
hg18149901
hg17149901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751428
Supporting Variants
SamplesBEC_728
Known GenesLOC727924, OR4M2, OR4N3P, OR4N4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983883
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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