A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575874



Internal ID16363283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65792075..65892788hg38UCSC Ensembl
Innerchr17:63788193..63888906hg19UCSC Ensembl
Innerchr17:61218655..61319368hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38100714
hg19100714
hg18100714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875822
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575874
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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