A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574794



Internal ID16015517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36202819..36211948hg38UCSC Ensembl
Innerchr17:34530219..34539350hg19UCSC Ensembl
Innerchr17:31554332..31563463hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg389130
hg199132
hg189132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5544n54
Supporting Variantsnssv869962, nssv869955, nssv869958, nssv869956, nssv869963, nssv869961, nssv869957, nssv869960, nssv869959
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574794
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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