A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1045977
Internal ID
18788508
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr10:46428386..46481242
hg38
UCSC
Ensembl
Inner
chr10:47068215..47121369
hg19
UCSC
Ensembl
Inner
chr10:46488221..46541375
hg18
UCSC
Ensembl
Cytoband
10q11.22
Allele length
Assembly
Allele length
hg38
52857
hg19
53155
hg18
53155
Variant Type
CNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv815n100
Supporting Variants
nssv3519401
,
nssv3705906
,
nssv3517303
,
nssv3514797
,
nssv3512899
,
nssv3507197
,
nssv3519194
,
nssv3508583
Samples
Known Genes
LINC00842
,
LOC100996758
,
NPY4R
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)
nsv1045977
Frequency
Sample Size
29084
Observed Gain
7
Observed Loss
1
Observed Complex
0
Frequency
n/a
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