A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064679



Internal ID19153898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6392639..6411858hg38UCSC Ensembl
Innerchr17:6295959..6315178hg19UCSC Ensembl
Innerchr17:6236683..6255902hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3819220
hg1919220
hg1819220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3094n100
Supporting Variantsnssv3560322, nssv3719159
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)nsv1064679
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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