A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058111



Internal ID19147330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6390555..6408947hg38UCSC Ensembl
Innerchr17:6293875..6312267hg19UCSC Ensembl
Innerchr17:6234599..6252991hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3818393
hg1918393
hg1818393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3094n100
Supporting Variantsnssv3560311
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)nsv1058111
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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