A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574799



Internal ID16015522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36202819..36231368hg38UCSC Ensembl
Innerchr17:34530219..34558811hg19UCSC Ensembl
Innerchr17:31554332..31582924hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3828550
hg1928593
hg1828593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5547n54
Supporting Variantsnssv869972
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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