A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058494



Internal ID19147713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27068665..27128159hg38UCSC Ensembl
Innerchr17:25395691..25455185hg19UCSC Ensembl
Innerchr17:22419818..22479312hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3859495
hg1959495
hg1859495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561035
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058494
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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