A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567846



Internal ID18866127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79363311..79471877hg38UCSC Ensembl
Innerchr17:77359393..77467959hg19UCSC Ensembl
Innerchr17:74870988..74979554hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38108567
hg19108567
hg18108567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056051
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)nssv3567846
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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