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: nsv602823
Internal ID
16043546
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr6:33086269..33086898
hg38
UCSC
Ensembl
Inner
chr6:33054046..33054675
hg19
UCSC
Ensembl
Inner
chr6:33162024..33162653
hg18
UCSC
Ensembl
Cytoband
6p21.32
Allele length
Assembly
Allele length
hg38
630
hg19
630
hg18
630
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
Supporting Variants
nssv1057627
,
nssv1057630
,
nssv1057629
,
nssv1057628
,
nssv1057631
,
nssv1057634
,
nssv1057633
,
nssv1057632
,
nssv1057635
,
nssv1057636
Samples
Known Genes
HLA-DPB1
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)
nsv602823
Frequency
Sample Size
17421
Observed Gain
0
Observed Loss
10
Observed Complex
0
Frequency
n/a
Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage
disclaimer