A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759478



Internal ID9634937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152742157..152913595hg38UCSC Ensembl
Innerchr6:153063292..153234730hg19UCSC Ensembl
Innerchr6:153104985..153276423hg18UCSC Ensembl
Innerchr6:153155406..153326844hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38171439
hg19171439
hg18171439
hg17171439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758086
SamplesNA18573
Known GenesVIP
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)esv2759478
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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