A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv586258
Internal ID
16026981
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr20:54031291..54041462
hg38
UCSC
Ensembl
Inner
chr20:52647830..52658001
hg19
UCSC
Ensembl
Inner
chr20:52081237..52091408
hg18
UCSC
Ensembl
Cytoband
20q13.2
Allele length
Assembly
Allele length
hg38
10172
hg19
10172
hg18
10172
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv7608n54
Supporting Variants
nssv941503
,
nssv941502
,
nssv941501
,
nssv941496
,
nssv941498
,
nssv941497
,
nssv941499
,
nssv941500
,
nssv941504
,
nssv941505
Samples
Known Genes
BCAS1
Method
SNP array
Analysis
Illumina SNP array copy number analysis
Platform
Not reported
Comments
Reference
Cooper_et_al_2011
Pubmed ID
21841781
Accession Number(s)
nsv586258
Frequency
Sample Size
17421
Observed Gain
0
Observed Loss
10
Observed Complex
0
Frequency
n/a
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