A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599879



Internal ID18551474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:20958000..21000405hg38UCSC Ensembl
Innerchr21:22330317..22372723hg19UCSC Ensembl
Innerchr21:21252188..21294594hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3842406
hg1942407
hg1842407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057774
Supporting Variants
Samples
Known GenesNCAM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599879
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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