A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732569



Internal ID19030850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13197951..13883095hg38UCSC Ensembl
Innerchr21:14570272..15255416hg19UCSC Ensembl
Innerchr21:13492143..14177287hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38685145
hg19685145
hg18685145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057563
Supporting Variants
Samples
Known GenesC21orf15, LOC100288966, 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)nssv3732569
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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