A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585288



Internal ID18883569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13221902..13715716hg38UCSC Ensembl
Innerchr21:14594223..15088037hg19UCSC Ensembl
Innerchr21:13516094..14009908hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38493815
hg19493815
hg18493815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064893
Supporting Variants
Samples
Known GenesLOC100288966, MIR3156-3, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585288
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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