A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1007788
Internal ID
18750319
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr3:151794802..151830691
hg38
UCSC
Ensembl
Inner
chr3:151512590..151548479
hg19
UCSC
Ensembl
Inner
chr3:152995280..153031169
hg18
UCSC
Ensembl
Cytoband
3q25.1
Allele length
Assembly
Allele length
hg38
35890
hg19
35890
hg18
35890
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv4920n100
Supporting Variants
nssv3606330
,
nssv3606329
,
nssv3741536
,
nssv3606328
,
nssv3606326
,
nssv3606331
,
nssv3741537
,
nssv3741538
,
nssv3606327
Samples
Known Genes
AADAC
,
MIR548H2
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)
nsv1007788
Frequency
Sample Size
29084
Observed Gain
0
Observed Loss
9
Observed Complex
0
Frequency
n/a
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