A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065859



Internal ID19155078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14497561..14521563hg38UCSC Ensembl
Innerchr17:14400878..14424880hg19UCSC Ensembl
Innerchr17:14341603..14365605hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3824003
hg1924003
hg1824003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3103n100
Supporting Variantsnssv3560377
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)nsv1065859
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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