A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1039256
Internal ID
18781787
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr16:6608311..6638066
hg38
UCSC
Ensembl
Inner
chr16:6658312..6688067
hg19
UCSC
Ensembl
Inner
chr16:6598313..6628068
hg18
UCSC
Ensembl
Cytoband
16p13.2
Allele length
Assembly
Allele length
hg38
29756
hg19
29756
hg18
29756
Variant Type
CNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv2704n100
Supporting Variants
nssv3557038
,
nssv3557041
,
nssv3557039
,
nssv3718849
,
nssv3557040
,
nssv3718848
,
nssv3557035
,
nssv3718847
,
nssv3557036
,
nssv3557037
Samples
Known Genes
RBFOX1
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)
nsv1039256
Frequency
Sample Size
29084
Observed Gain
10
Observed Loss
0
Observed Complex
0
Frequency
n/a
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