A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057490



Internal ID19146709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77043982..77081209hg38UCSC Ensembl
Innerchr17:75040064..75077291hg19UCSC Ensembl
Innerchr17:72551659..72588886hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3837228
hg1937228
hg1837228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567811
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)nsv1057490
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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