A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1045360
Internal ID
18787891
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr15:34408470..34563605
hg38
UCSC
Ensembl
Inner
chr15:34700671..34855806
hg19
UCSC
Ensembl
Inner
chr15:32487963..32643098
hg18
UCSC
Ensembl
Cytoband
15q14
Allele length
Assembly
Allele length
hg38
155136
hg19
155136
hg18
155136
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv2554n100
Supporting Variants
nssv3721753
,
nssv3721754
,
nssv3721752
,
nssv3721751
,
nssv3548886
,
nssv3548884
,
nssv3548885
Samples
Known Genes
GOLGA8A
,
GOLGA8B
,
MIR1233-1
,
MIR1233-2
Method
SNP array
Analysis
Affymetrix SNP array copy number analysis
Platform
Affymetrix SNP Array 6.0
Comments
Reference
Coe_et_al_2014
Pubmed ID
25217958
Accession Number(s)
nsv1045360
Frequency
Sample Size
29084
Observed Gain
0
Observed Loss
7
Observed Complex
0
Frequency
n/a
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