A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984550



Internal ID12630484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22037985..22289785hg38UCSC Ensembl
Innerchr15:22325936..22577736hg19UCSC Ensembl
Innerchr15:19827300..20079100hg18UCSC Ensembl
Innerchr15:19827300..20079100hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38251801
hg19251801
hg18251801
hg17251801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751354
Supporting Variants
SamplesBEC_718
Known GenesLOC727924, OR4M2, OR4N3P, OR4N4, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984550
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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