A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561034



Internal ID18859315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27060774..27098348hg38UCSC Ensembl
Innerchr17:25387800..25425374hg19UCSC Ensembl
Innerchr17:22411927..22449501hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3837575
hg1937575
hg1837575
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056471
Supporting Variants
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)nssv3561034
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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