A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574321



Internal ID16015044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6855195..6972341hg38UCSC Ensembl
Innerchr17:6758514..6875660hg19UCSC Ensembl
Innerchr17:6699238..6816384hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38117147
hg19117147
hg18117147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5440n54
Supporting Variantsnssv866671
Samples
Known GenesALOX12P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574321
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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