A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561121



Internal ID18512716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36062064..36134107hg38UCSC Ensembl
Innerchr17:34389424..34461489hg19UCSC Ensembl
Innerchr17:31413537..31485602hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3872044
hg1972066
hg1872066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059828
Supporting Variants
Samples
Known GenesCCL18, CCL3, CCL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561121
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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