A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560935



Internal ID18859216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21406105..21638845hg38UCSC Ensembl
Innerchr17:21309417..21542085hg19UCSC Ensembl
Innerchr17:21250010..21482678hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38232741
hg19232669
hg18232669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056000
Supporting Variants
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)nssv3560935
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