A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066228



Internal ID19155447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79191761..79238441hg38UCSC Ensembl
Innerchr17:77187843..77234523hg19UCSC Ensembl
Innerchr17:74699438..74746118hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3846681
hg1946681
hg1846681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3287n100
Supporting Variantsnssv3567831
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)nsv1066228
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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