A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv575968
Internal ID
16016691
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr17:72819272..72821975
hg38
UCSC
Ensembl
Inner
chr17:70815411..70818114
hg19
UCSC
Ensembl
Inner
chr17:68327006..68329709
hg18
UCSC
Ensembl
Cytoband
17q24.3
Allele length
Assembly
Allele length
hg38
2704
hg19
2704
hg18
2704
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv5764n54
Supporting Variants
nssv875953
,
nssv875954
,
nssv875956
,
nssv875951
,
nssv875957
,
nssv875952
,
nssv875955
,
nssv875958
,
nssv875950
,
nssv875959
Samples
Known Genes
SLC39A11
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)
nsv575968
Frequency
Sample Size
17421
Observed Gain
0
Observed Loss
10
Observed Complex
0
Frequency
n/a
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