A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587015



Internal ID16374424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13585652..14076239hg38UCSC Ensembl
Innerchr21:14957973..15448560hg19UCSC Ensembl
Innerchr21:13879844..14370431hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38490588
hg19490588
hg18490588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7757n54
Supporting Variantsnssv944918, nssv944917
Samples
Known GenesANKRD20A11P, C21orf15, LOC100288966, MIR8069, POTED
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587015
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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