A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585294



Internal ID18883575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13221902..13765257hg38UCSC Ensembl
Innerchr21:14594223..15137578hg19UCSC Ensembl
Innerchr21:13516094..14059449hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38543356
hg19543356
hg18543356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064798
Supporting Variants
Samples
Known GenesLOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585294
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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