A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758212



Internal ID9980289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20397790..20609679hg38UCSC Ensembl
Innerchr10:20686719..20898608hg19UCSC Ensembl
Innerchr10:20726725..20938614hg18UCSC Ensembl
Innerchr10:20726725..20938614hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38211890
hg19211890
hg18211890
hg17211890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759739
Supporting Variantsessv22942, essv21042, essv22075, essv23352, essv22825, essv22353, essv19766, essv20623, essv24062, essv24137, essv7559, essv21297, essv22764, essv22003, essv2258, essv20187, essv7789, essv1968, essv5176, essv2966, essv24469, essv18191, essv22894, essv18961, essv7359, essv6908, essv18704, essv16720, essv4600, essv1269, essv6376, essv226, essv18592, essv4411, essv23678, essv17653, essv7719, essv20300, essv20963, essv14203, essv6130, essv21554, essv23563, essv7187, essv23060, essv21679, essv19645, essv5402, essv6283, essv4832, essv4641, essv20381, essv21777, essv4901
SamplesNA11995, NA18524, NA18561, NA18545, NA12004, NA12801, NA12248, NA18959, NA18633, NA12750, NA12155, NA07357, NA18563, NA12812, NA10835, NA18995, NA18558, NA18547, NA06993, NA18611, NA12005, NA07019, NA18966, NA10855, NA10847, NA18605, NA12760, NA10863, NA18572, NA18948, NA18981, NA12234, NA18573, NA19142, NA10830, NA12056, NA18532, NA12239, NA12144, NA06985, NA18570, NA06991, NA11881, NA18540, NA12057, NA10859, NA19140, NA12873, NA12874, NA18594, NA18636, NA07056, NA12154, NA11832
Known GenesMIR4675
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)esv2758212
Frequency
Sample Size270
Observed Gain0
Observed Loss54
Observed Complex0
Frequencyn/a


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