A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv573391
Internal ID
16014114
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr16:83162838..83174417
hg38
UCSC
Ensembl
Inner
chr16:83196443..83208022
hg19
UCSC
Ensembl
Inner
chr16:81753944..81765523
hg18
UCSC
Ensembl
Cytoband
16q23.3
Allele length
Assembly
Allele length
hg38
11580
hg19
11580
hg18
11580
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv5256n54
Supporting Variants
nssv861974
,
nssv861975
,
nssv861978
,
nssv861976
,
nssv861969
,
nssv861970
,
nssv861977
,
nssv861973
,
nssv861972
,
nssv861971
Samples
Known Genes
CDH13
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)
nsv573391
Frequency
Sample Size
17421
Observed Gain
0
Observed Loss
10
Observed Complex
0
Frequency
n/a
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