A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574279



Internal ID16361688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:5688844..5693567hg38UCSC Ensembl
Innerchr17:5592164..5596887hg19UCSC Ensembl
Innerchr17:5532888..5537611hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg384724
hg194724
hg184724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5432n54
Supporting Variantsnssv866566
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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