A curated catalogue of human genomic structural variation




Variant Details

Variant: essv20938



Internal ID9960198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156366694..156633173hg38UCSC Ensembl
Innerchr7:156159388..156425867hg19UCSC Ensembl
Innerchr7:155852149..156118628hg18UCSC Ensembl
Innerchr7:155658864..155925343hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38266480
hg19266480
hg18266480
hg17266480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758143
Supporting Variants
SamplesNA12801
Known GenesLINC00244, LINC01006, LOC285889
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)essv20938
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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