A curated catalogue of human genomic structural variation
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Variant Details
Variant: esv3892025
Internal ID
18839735
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr11:71675753..71814755
hg38
UCSC
Ensembl
Outer
chr11:71570814..71849534
hg38
UCSC
Ensembl
Inner
chr11:71386799..71525801
hg19
UCSC
Ensembl
Outer
chr11:71281860..71560580
hg19
UCSC
Ensembl
Inner
chr11:71064447..71203449
hg18
UCSC
Ensembl
Outer
chr11:70959508..71238228
hg18
UCSC
Ensembl
Cytoband
11q13.4
Allele length
Assembly
Allele length
hg38
278721
hg19
278721
hg18
278721
Variant Type
CNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
Supporting Variants
essv25791993
,
essv25791351
,
essv25792156
,
essv25792433
,
essv25790929
,
essv25791859
Samples
Known Genes
ALG1L9P
,
DEFB108B
,
FAM86C1
,
KRTAP5-11
,
ZNF705E
Method
SNP array
Analysis
Platform
Illumina HumanHap 610
Comments
Reference
Suktitipat_et_al_2014
Pubmed ID
25118596
Accession Number(s)
esv3892025
Frequency
Sample Size
3017
Observed Gain
6
Observed Loss
0
Observed Complex
0
Frequency
n/a
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