A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574780



Internal ID16015503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36181006..36212480hg38UCSC Ensembl
Innerchr17:34508382..34539882hg19UCSC Ensembl
Innerchr17:31532495..31563995hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3831475
hg1931501
hg1831501
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869905, nssv869906, nssv869908, nssv869907, nssv869909, nssv869911, nssv869910
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)nsv574780
Frequency
Sample Size17421
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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