A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063911



Internal ID19153130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21399695..21615833hg38UCSC Ensembl
Innerchr17:21303007..21519100hg19UCSC Ensembl
Innerchr17:21243600..21459693hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38216139
hg19216094
hg18216094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3124n100
Supporting Variantsnssv3560929
Samples
Known GenesC17orf51, KCNJ12, KCNJ18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063911
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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