A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1044637
Internal ID
18787168
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr13:24445874..24465528
hg38
UCSC
Ensembl
Inner
chr13:25020012..25039666
hg19
UCSC
Ensembl
Inner
chr13:23918012..23937666
hg18
UCSC
Ensembl
Cytoband
13q12.12
Allele length
Assembly
Allele length
hg38
19655
hg19
19655
hg18
19655
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv1617n100
Supporting Variants
nssv3523169
,
nssv3523166
,
nssv3523172
,
nssv3523167
,
nssv3523165
,
nssv3523170
,
nssv3523173
,
nssv3523168
,
nssv3523171
Samples
Known Genes
PARP4
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)
nsv1044637
Frequency
Sample Size
29084
Observed Gain
0
Observed Loss
9
Observed Complex
0
Frequency
n/a
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