A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586818



Internal ID18538413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:218208654..218248378hg38UCSC Ensembl
Innerchr2:219073377..219113101hg19UCSC Ensembl
Innerchr2:218781622..218821346hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3839725
hg1939725
hg1839725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013137
Supporting Variants
Samples
Known GenesARPC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586818
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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