A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061019



Internal ID18803550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37070404..37117674hg38UCSC Ensembl
Innerchr17:35427696..35474608hg19UCSC Ensembl
Innerchr17:32501809..32548721hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3847271
hg1946913
hg1846913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562542
Samples
Known GenesACACA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061019
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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