A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574783



Internal ID16015506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36181006..36235529hg38UCSC Ensembl
Innerchr17:34508382..34562973hg19UCSC Ensembl
Innerchr17:31532495..31587086hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3854524
hg1954592
hg1854592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869916
Samples
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574783
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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