A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066406



Internal ID19155625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27036360..27089572hg38UCSC Ensembl
Innerchr17:25363386..25416598hg19UCSC Ensembl
Innerchr17:22387513..22440725hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3853213
hg1953213
hg1853213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3720042
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)nsv1066406
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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