A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10140



Internal ID9974341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85107707..85341481hg38UCSC Ensembl
Innerchr15:85650938..85884712hg19UCSC Ensembl
Innerchr15:83451942..83685716hg18UCSC Ensembl
Innerchr15:83451942..83685716hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38233775
hg19233775
hg18233775
hg17233775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758394
Supporting Variants
SamplesNA19130
Known GenesLOC440300, LOC642423, PDE8A
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv10140
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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