A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12728



Internal ID9610034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:70144362..70865721hg38UCSC Ensembl
Innerchr5:69440189..70161548hg19UCSC Ensembl
Innerchr5:69475945..70197304hg18UCSC Ensembl
Innerchr5:69475945..70197304hg17UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38721360
hg19721360
hg18721360
hg17721360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757998
Supporting Variants
SamplesNA18914
Known GenesGTF2H2B, GTF2H2C, GTF2H2D, GUSBP9, LOC441081, SMA4, SMA5
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)essv12728
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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