A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527899



Internal ID15455192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79085706..79165563hg38UCSC Ensembl
Innerchr17:77081788..77161645hg19UCSC Ensembl
Innerchr17:74593383..74673240hg18UCSC Ensembl
Innerchr17:74593383..74673240hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3879858
hg1979858
hg1879858
hg1779858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704403
Samples
Known GenesENGASE, RBFOX3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527899
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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