A curated catalogue of human genomic structural variation
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Variant Details
Variant: esv3890980
Internal ID
18838690
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr6:162176920..162318733
hg38
UCSC
Ensembl
Outer
chr6:162163721..162329393
hg38
UCSC
Ensembl
Inner
chr6:162597952..162739765
hg19
UCSC
Ensembl
Outer
chr6:162584753..162750425
hg19
UCSC
Ensembl
Inner
chr6:162517942..162659755
hg18
UCSC
Ensembl
Outer
chr6:162504743..162670415
hg18
UCSC
Ensembl
Cytoband
6q26
Allele length
Assembly
Allele length
hg38
165673
hg19
165673
hg18
165673
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
Supporting Variants
essv25779043
,
essv25780612
,
essv25781252
,
essv25798764
,
essv25784217
,
essv25783750
,
essv25799890
,
essv25797762
,
essv25796150
,
essv25797753
Samples
Known Genes
PARK2
Method
SNP array
Analysis
Platform
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
Reference
Suktitipat_et_al_2014
Pubmed ID
25118596
Accession Number(s)
esv3890980
Frequency
Sample Size
3017
Observed Gain
0
Observed Loss
10
Observed Complex
0
Frequency
n/a
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