A curated catalogue of human genomic structural variation




Variant Details

Variant: essv21861



Internal ID9620182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21802686..22976671hg38UCSC Ensembl
Innerchr19:21985488..23159473hg19UCSC Ensembl
Innerchr19:21777328..22951313hg18UCSC Ensembl
Innerchr19:21777328..22951313hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381173986
hg191173986
hg181173986
hg171173986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758491, esv2758490
Supporting Variants
SamplesNA11839
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
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)essv21861
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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