A curated catalogue of human genomic structural variation
About the Project
Genome Browser
Downloads
Query Tool
Links
Submissions
Statistics
Contact Us
FAQ
Training Resources
Variant Details
Variant: nsv615398
Internal ID
16056121
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr9:128688840..128690282
hg38
UCSC
Ensembl
Inner
chr9:131451119..131452561
hg19
UCSC
Ensembl
Inner
chr9:130490940..130492382
hg18
UCSC
Ensembl
Cytoband
9q34.11
Allele length
Assembly
Allele length
hg38
1443
hg19
1443
hg18
1443
Variant Type
CNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv12884n54
Supporting Variants
nssv1143232
,
nssv1143240
,
nssv1143237
,
nssv1143234
,
nssv1143235
,
nssv1143239
,
nssv1143241
,
nssv1143236
,
nssv1143238
,
nssv1143233
Samples
Known Genes
SET
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)
nsv615398
Frequency
Sample Size
17421
Observed Gain
10
Observed Loss
0
Observed Complex
0
Frequency
n/a
Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage
disclaimer