A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981735



Internal ID12625921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22037966..22289825hg38UCSC Ensembl
Innerchr15:22325917..22577776hg19UCSC Ensembl
Innerchr15:19827281..20079140hg18UCSC Ensembl
Innerchr15:19827281..20079140hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38251860
hg19251860
hg18251860
hg17251860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751362
Supporting Variants
SamplesBEC_330
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)essv6981735
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer