A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560965



Internal ID18859246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21437988..21609743hg38UCSC Ensembl
Innerchr17:21341300..21513010hg19UCSC Ensembl
Innerchr17:21281893..21453603hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38171756
hg19171711
hg18171711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059024
Supporting Variants
Samples
Known GenesC17orf51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560965
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