A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575887



Internal ID16363296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66074410..66153058hg38UCSC Ensembl
Innerchr17:64070528..64149176hg19UCSC Ensembl
Innerchr17:61500990..61579638hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3878649
hg1978649
hg1878649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5748n54
Supporting Variantsnssv875832
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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