A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055429



Internal ID18797960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34299853..34516938hg38UCSC Ensembl
Innerchr21:35672153..35889236hg19UCSC Ensembl
Innerchr21:34594023..34811106hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38217086
hg19217084
hg18217084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600134
Samples
Known GenesC21orf140, KCNE1, KCNE2, RCAN1, SMIM11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055429
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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