A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574788



Internal ID16015511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36201388..36212480hg38UCSC Ensembl
Innerchr17:34528788..34539882hg19UCSC Ensembl
Innerchr17:31552901..31563995hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3811093
hg1911095
hg1811095
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869929, nssv869928, nssv869927
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574788
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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