A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1062151
Internal ID
18804682
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr17:46088437..46148520
hg38
UCSC
Ensembl
Inner
chr17:44165803..44225886
hg19
UCSC
Ensembl
Inner
chr17:41521621..41581663
hg18
UCSC
Ensembl
Cytoband
17q21.31
Allele length
Assembly
Allele length
hg38
60084
hg19
60084
hg18
60043
Variant Type
CNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv3183n100
Supporting Variants
nssv3546180
,
nssv3546179
,
nssv3546177
,
nssv3546183
,
nssv3546185
,
nssv3546178
,
nssv3720306
,
nssv3546184
,
nssv3546181
,
nssv3546182
Samples
Known Genes
KANSL1
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)
nsv1062151
Frequency
Sample Size
29084
Observed Gain
10
Observed Loss
0
Observed Complex
0
Frequency
n/a
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