A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574771



Internal ID16015494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36118154..36215910hg38UCSC Ensembl
Innerchr17:34445545..34543364hg19UCSC Ensembl
Innerchr17:31469658..31567477hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3897757
hg1997820
hg1897820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5538n54
Supporting Variantsnssv869895
Samples
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2, TBC1D3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574771
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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