A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567845



Internal ID18866126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79363311..79430942hg38UCSC Ensembl
Innerchr17:77359393..77427024hg19UCSC Ensembl
Innerchr17:74870988..74938619hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3867632
hg1967632
hg1867632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061588
Supporting Variants
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)nssv3567845
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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