A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574668



Internal ID16015391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31168877..31228337hg38UCSC Ensembl
Innerchr17:29495895..29555355hg19UCSC Ensembl
Innerchr17:26520021..26579481hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3859461
hg1959461
hg1859461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869523
Samples
Known GenesNF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574668
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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