A curated catalogue of human genomic structural variation
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Variant Details
Variant: esv2759786
Internal ID
9635245
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr10:122503559..122695299
hg38
UCSC
Ensembl
Inner
chr10:124263075..124454815
hg19
UCSC
Ensembl
Inner
chr10:124253065..124444805
hg18
UCSC
Ensembl
Inner
chr10:124253065..124444805
hg17
UCSC
Ensembl
Cytoband
10q26.13
Allele length
Assembly
Allele length
hg38
191741
hg19
191741
hg18
191741
hg17
191741
Variant Type
CNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
Supporting Variants
esv2758242
Samples
NA18508, NA18526, NA18563, NA19201, NA19119, NA18942, NA19130, NA19172, NA19209, NA19120, NA10831, NA18956, NA18948, NA18981, NA18566, NA12264, NA18978, NA18952, NA19173, NA19116, NA18623, NA18577, NA18620
Known Genes
DMBT1
,
HTRA1
Method
BAC aCGH
Analysis
Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
Platform
Agilent
Comments
Reference
Redon_et_al_2006
Pubmed ID
17122850
Accession Number(s)
esv2759786
Frequency
Sample Size
270
Observed Gain
10
Observed Loss
13
Observed Complex
0
Frequency
n/a
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