A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066469



Internal ID19155688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22194522..22720229hg38UCSC Ensembl
Innerchr17:21721128..22219556hg19UCSC Ensembl
Innerchr17:21645255..22143683hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38525708
hg19498429
hg18498429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3131n100
Supporting Variantsnssv3561015
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066469
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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