A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058697



Internal ID19147916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79363311..79423410hg38UCSC Ensembl
Innerchr17:77359393..77419492hg19UCSC Ensembl
Innerchr17:74870988..74931087hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3860100
hg1960100
hg1860100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3289n100
Supporting Variantsnssv3567844
Samples
Known GenesRBFOX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058697
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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