A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575886



Internal ID16363295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66074410..66151258hg38UCSC Ensembl
Innerchr17:64070528..64147376hg19UCSC Ensembl
Innerchr17:61500990..61577838hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3876849
hg1976849
hg1876849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5748n54
Supporting Variantsnssv875831, nssv875830
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575886
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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