A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869857



Internal ID16163813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36104732..36154379hg38UCSC Ensembl
Innerchr17:34432125..34481759hg19UCSC Ensembl
Innerchr17:31456238..31505872hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3849648
hg1949635
hg1849635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574758
Supporting Variants
Samples
Known GenesCCL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869857
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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