A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058878



Internal ID18801409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6384798..6411858hg38UCSC Ensembl
Innerchr17:6288118..6315178hg19UCSC Ensembl
Innerchr17:6228842..6255902hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3827061
hg1927061
hg1827061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3093n100
Supporting Variantsnssv3560305
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)nsv1058878
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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