A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575916



Internal ID16363325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67969488..67979576hg38UCSC Ensembl
Innerchr17:65965604..65975692hg19UCSC Ensembl
Innerchr17:63396066..63406154hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3810089
hg1910089
hg1810089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875896
Samples
Known GenesBPTF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575916
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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