A curated catalogue of human genomic structural variation
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Variant Details
Variant: esv3892678
Internal ID
18836812
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr15:42130892..42138944
hg38
UCSC
Ensembl
Outer
chr15:42130892..42142055
hg38
UCSC
Ensembl
Inner
chr15:42423090..42431142
hg19
UCSC
Ensembl
Outer
chr15:42423090..42434253
hg19
UCSC
Ensembl
Inner
chr15:40210382..40218434
hg18
UCSC
Ensembl
Outer
chr15:40210382..40221545
hg18
UCSC
Ensembl
Cytoband
15q15.1
Allele length
Assembly
Allele length
hg38
11164
hg19
11164
hg18
11164
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
Supporting Variants
essv25780063
,
essv25796312
,
essv25798316
,
essv25798470
,
essv25797675
,
essv25796308
,
essv25780444
,
essv25781615
,
essv25786664
,
essv25785465
Samples
Known Genes
PLA2G4F
Method
SNP array
Analysis
Platform
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
Reference
Suktitipat_et_al_2014
Pubmed ID
25118596
Accession Number(s)
esv3892678
Frequency
Sample Size
3017
Observed Gain
0
Observed Loss
10
Observed Complex
0
Frequency
n/a
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