A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060861



Internal ID18803392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:43338154..43791949hg38UCSC Ensembl
Innerchr17:41415522..41869317hg19UCSC Ensembl
Innerchr17:38771048..39224843hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38453796
hg19453796
hg18453796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545119, nssv3545120
Samples
Known GenesARL4D, C17orf105, DHX8, DUSP3, ETV4, LINC00910, MEOX1, MIR2117, SOST
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060861
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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