A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868357



Internal ID16162313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15131524..15157065hg38UCSC Ensembl
Innerchr17:15034841..15060382hg19UCSC Ensembl
Innerchr17:14975566..15001107hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3825542
hg1925542
hg1825542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574435
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868357
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