A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1058621
Internal ID
18801152
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr20:14895232..14952238
hg38
UCSC
Ensembl
Inner
chr20:14875878..14932884
hg19
UCSC
Ensembl
Inner
chr20:14823878..14880884
hg18
UCSC
Ensembl
Cytoband
20p12.1
Allele length
Assembly
Allele length
hg38
57007
hg19
57007
hg18
57007
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv4272n100
Supporting Variants
nssv3737157
,
nssv3599603
,
nssv3737156
,
nssv3599601
,
nssv3737155
,
nssv3737154
,
nssv3599600
,
nssv3599602
Samples
Known Genes
MACROD2
,
MACROD2-AS1
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)
nsv1058621
Frequency
Sample Size
29084
Observed Gain
0
Observed Loss
8
Observed Complex
0
Frequency
n/a
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