A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061358



Internal ID18803889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34339322..34534919hg38UCSC Ensembl
Innerchr21:35711621..35907217hg19UCSC Ensembl
Innerchr21:34633491..34829087hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38195598
hg19195597
hg18195597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4426n100
Supporting Variantsnssv3600135
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)nsv1061358
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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