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: nsv594946
Internal ID
16035669
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr4:101039102..101039600
hg38
UCSC
Ensembl
Inner
chr4:101960259..101960757
hg19
UCSC
Ensembl
Inner
chr4:102179282..102179780
hg18
UCSC
Ensembl
Cytoband
4q23
Allele length
Assembly
Allele length
hg38
499
hg19
499
hg18
499
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv9180n54
Supporting Variants
nssv1003444
,
nssv1003445
,
nssv1003446
,
nssv1003443
,
nssv1003441
,
nssv1003448
,
nssv1003449
,
nssv1003447
,
nssv1003442
Samples
Known Genes
PPP3CA
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)
nsv594946
Frequency
Sample Size
17421
Observed Gain
0
Observed Loss
9
Observed Complex
0
Frequency
n/a
Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage
disclaimer