A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574789



Internal ID16015512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36201388..36214601hg38UCSC Ensembl
Innerchr17:34528788..34542055hg19UCSC Ensembl
Innerchr17:31552901..31566168hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3813214
hg1913268
hg1813268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5545n54
Supporting Variantsnssv869930
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574789
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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