A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574362



Internal ID16361771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11331302..11417075hg38UCSC Ensembl
Innerchr17:11234619..11320392hg19UCSC Ensembl
Innerchr17:11175344..11261117hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3885774
hg1985774
hg1885774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866783
Samples
Known GenesSHISA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574362
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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