A curated catalogue of human genomic structural variation




Variant Details

Variant: esv23518



Internal ID11040751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99966510..100027788hg38UCSC Ensembl
Innerchr7:99564133..99625411hg19UCSC Ensembl
Innerchr7:99402069..99463347hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3861279
hg1961279
hg1861279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv19900
SamplesNA15510
Known GenesAZGP1, AZGP1P1, ZKSCAN1
MethodOligo aCGH
AnalysisSegment log2 ratios from each sample. This was done running the GADA algorithm (Pique-Regi et al., 2008) using the options "-M 10 -T 10 -a 2.5". Filter non-CNV segments using intensity thresholds. Merge remaining CNV "calls" within each sample. Adjacent calls of the same direction (gain or loss) are merged if both: the distance between calls is less than 10kb, and the distance between calls is less than 10% of the size of the largest of the two calls.
PlatformSanger H. Sapiens 42mCGH Array 5781_53 726K v1
Comments
ReferenceConrad_et_al_2009
Pubmed ID19812545
Accession Number(s)esv23518
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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