A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587580



Internal ID16374989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41928931..41932756hg38UCSC Ensembl
Innerchr21:43349040..43352865hg19UCSC Ensembl
Innerchr21:42222109..42225934hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383826
hg193826
hg183826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7853n54
Supporting Variantsnssv947158
Samples
Known GenesC2CD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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