A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574772



Internal ID16015495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36123619..36198514hg38UCSC Ensembl
Innerchr17:34451005..34525914hg19UCSC Ensembl
Innerchr17:31475118..31550027hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3874896
hg1974910
hg1874910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5536n54
Supporting Variantsnssv869896
Samples
Known GenesCCL3L1, CCL3L3, TBC1D3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574772
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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