A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570916



Internal ID16011639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101798224..101829176hg38UCSC Ensembl
Innerchr15:102338427..102369379hg19UCSC Ensembl
Innerchr15:100155950..100186902hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3830953
hg1930953
hg1830953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851223, nssv851222, nssv851225, nssv851224
Samples
Known GenesOR4F15, OR4F6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570916
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer