A curated catalogue of human genomic structural variation




Variant Details

Variant: essv21834



Internal ID9956792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65515626..65743618hg38UCSC Ensembl
Innerchr7:64980539..65208605hg19UCSC Ensembl
Innerchr7:64617974..64846040hg18UCSC Ensembl
Innerchr7:64424689..64652755hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38227993
hg19228067
hg18228067
hg17228067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758117
Supporting Variants
SamplesNA11839
Known GenesINTS4L2, LOC441242
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)essv21834
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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