A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063726



Internal ID18806257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13197951..13944123hg38UCSC Ensembl
Innerchr21:14570272..15316444hg19UCSC Ensembl
Innerchr21:13492143..14238315hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38746173
hg19746173
hg18746173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4378n100
Supporting Variantsnssv3732572
Samples
Known GenesANKRD20A11P, C21orf15, 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)nsv1063726
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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