A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733450



Internal ID18685045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38742206..38818670hg38UCSC Ensembl
Innerchr21:40114130..40190594hg19UCSC Ensembl
Innerchr21:39036000..39112464hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3876465
hg1976465
hg1876465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058591
Supporting Variants
Samples
Known GenesETS2, LINC00114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733450
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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