A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063941



Internal ID18806472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16453772..16520784hg38UCSC Ensembl
Innerchr17:16357086..16424098hg19UCSC Ensembl
Innerchr17:16297811..16364823hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3867013
hg1967013
hg1867013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560425
Samples
Known GenesFAM211A, FAM211A-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063941
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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